Part II: Irony of Profit-Driven HealthCare Systems: Are they keeping us just sick enough?💸💰

Do you ever wonder: If CVS and Walgreens (convenience stores, grocery stores, etc) cared about our health, why they wouldn’t stock the shelves full of clean products?

Instead, ingredients in every single aisle are scientifically known to drive so many diseases- from ADHD, Asthma, Alzheimer’s, Dementia, Mental Health problems, and Cancers.

Sick People bring in Big bucks.

In-store vaccinations, flu shots, prescription medications, OTC medications, and retail bring in $372 billion in annual revenue in 2023–2024 Walgreens Boots Alliance reported approximately $147 billion in annual revenue, largely driven by retail pharmacy operations.

“They make money on the flu shots. Money on the flu shots when they fail. Money on the products bought when getting shots and scrips in store. And money on the diseases driven by the ingredients in the products people buy.”

Let’s look at some examples.

Top dangerous ingredients on the shelves with links to disease.

Formaldehyde and FRPs

Formaldehyde itself is rarely listed outright in personal-care products sold at major drugstores like CVS and Walgreens, but it often appears indirectly through formaldehyde-releasing preservatives. These ingredients are added to shampoos, conditioners, lotions, body washes, soaps, and cosmetics to prevent bacterial growth.

Common examples include: DMDM hydantoin, diazolidinyl urea, imidazolidinyl urea, quaternium-15, and sodium hydroxymethylglycinate.

While these names may look unfamiliar on a label, they matter because they slowly release small amounts of formaldehyde over time — meaning repeated daily use across multiple products can lead to ongoing exposure, even when “formaldehyde” itself is never listed.

Health authorities including the National Cancer Institute, American Cancer Society, and the World Health Organization classify formaldehyde as a known human carcinogen, with long-term exposure linked to cancers such as leukemia and cancers of the nasal and upper respiratory passages, particularly in occupational or chronic-exposure settings.

Vaccines and shots that may contain (residual) formaldehyde due to the manufacturing process (not as an active ingredient). *This phrasing is commonly used by CDC/FDA-aligned sources and vaccine ingredient disclosures:

-Influenza (flu) vaccines Some inactivated flu shots may contain trace residual formaldehyde used to inactivate the virus (varies by formulation and manufacturer).

DTaP vaccines (Diphtheria, Tetanus, Pertussis – pediatric) Tdap vaccines (Tetanus, Diphtheria, Pertussis – adolescent/adult boosters) DT vaccines (Diphtheria, Tetanus)

Hepatitis A vaccines (e.g., Havrix, Vaqta) Combination Hepatitis A & B vaccine (Twinrix)

Hib vaccines (Haemophilus influenzae type b)

Polio vaccines (IPV) Some meningococcal vaccines (e.g., Menactra, Menveo) Certain combination pediatric vaccines (e.g., Pentacel, Kinrix — depending on components)

At lower levels, which are more typical of consumer products, formaldehyde and its releasers are well-documented skin sensitizers, frequently associated with allergic reactions, eczema, dermatitis, eye irritation, and respiratory symptoms — especially in children and people with asthma or sensitive skin. Because these preservatives can be found across multiple everyday products, researchers and public-health experts increasingly emphasize the issue of cumulative exposure, where small amounts add up over time.

In response to growing concern, CVS has publicly committed to removing formaldehyde-releasing preservatives from many of its own private-label personal-care brands, though this policy does not apply to all national brands sold on its shelves.

Walgreens has made more limited or product-specific claims, meaning shoppers may still encounter these ingredients depending on the brand and product line.

As a result, consumers who wish to minimize exposure are encouraged to read ingredients!

Note: Walgreens and CVS heavily donate to American Cancer Society and American Heart Association. *Links to WHO (World Economic Forum) *Part III: What is the WHO and how far does their Global Power Reach. … to be continued …

Alzheimer’s, Dementia and Anticholinergics

When people talk about medications and Alzheimer’s risk, the most consistent scientific signal isn’t about pain relievers like Tylenol—it’s about a group of drugs called anticholinergics. These medications block acetylcholine, a brain chemical that plays a key role in memory, learning, and attention.

Large observational studies summarized by the NIH and the National Institute on Aging have found that the more anticholinergic exposure a person has over time—the higher the dose, the longer the use, or the more of these drugs taken together—the higher the associated risk of developing dementia.

Common Anticholinergic Medications (Condensed List)

Over-the-Counter (OTC):

Diphenhydramine – Benadryl, Tylenol PM, Advil PM, Unisom SleepGels Doxylamine – Unisom SleepTabs, NyQuil Dimenhydrinate – Dramamine Meclizine – Bonine, Dramamine Less-Drowsy Chlorpheniramine / Brompheniramine – older cold & allergy products Promethazine – nausea, cough, motion sickness (Rx in U.S.)

Prescription – Bladder / Urinary:

Oxybutynin – Ditropan Tolterodine – Detrol Solifenacin – Vesicare Fesoterodine – Toviaz Trospium Darifenacin Flavoxate – Urispas

Prescription – GI & Motion:

Dicyclomine – Bentyl Scopolamine – motion sickness patch Glycopyrrolate Clidinium (often in combination GI meds)

Neurologic / Parkinson’s:

Benztropine – Cogentin Trihexyphenidyl Biperiden Atropine

Antidepressants with Strong Anticholinergic Effects:

Amitriptyline Imipramine Nortriptyline Paroxetine

Other Common Medications with Anticholinergic Burden:

Cyclobenzaprine – muscle relaxant Orphenadrine Certain antipsychotics – chlorpromazine, olanzapine, clozapine

What’s especially concerning is that this link has been seen even when the medications were used years before dementia symptoms appeared, suggesting the effects may be cumulative and long-lasting.

Anticholinergic drugs longer list

Prescription bladder medications are some of the most concerning anticholinergic drugs linked to dementia risk. Large, NIH-cited observational studies consistently identify antimuscarinic urinary medications—especially oxybutynin (Ditropan), and also tolterodine (Detrol), solifenacin (Vesicare), fesoterodine (Toviaz), and darifenacin (Enablex)—as having a strong anticholinergic burden. These drugs are often taken daily and long-term, which is exactly the exposure pattern associated with higher cumulative dementia risk. In several studies, bladder anticholinergics ranked among the highest contributors to anticholinergic cognitive burden, sometimes exceeding that of antidepressants or sleep aids.

Red 40 and ADHD

Red 40, also known as FD&C Red No. 40, is one of the most common artificial food dyes in the U.S., and it has raised particular concerns when it comes to children’s health. Some studies and anecdotal reports have suggested that Red 40 may exacerbate hyperactivity in children, particularly those with ADHD, and may contribute to behavioral issues. While the research is ongoing, concerns about artificial colorants have prompted some countries to require warning labels, and some parents opt to avoid it altogether.

Examples of products at CVS that list Red 40 include CVS Health Chewable Low Dose Aspirin (cherry flavor), Children’s Liquid Pain Reliever (berry flavor), Skittles Sour candies, Red Vines Red Ropes, and some AZO Urinary Tract Defense tablets.

Checking ingredient labels remains crucial, as formulations can vary.

Titanium Dioxide

Titanium dioxide is still widely used in the United States across foods, dietary supplements, medications, and personal-care products, despite offering no health benefit beyond cosmetic appeal.

It is added to make products look brighter, whiter, or more visually uniform — from candies and chewable tablets to vitamins, toothpaste, sunscreens, and makeup.

In many cases, consumers ingest or apply titanium dioxide daily without realizing it, as it often appears on ingredient labels under technical names such as titanium dioxide or CI 77891.

The concern is not its appearance, but its behavior in the body: titanium dioxide particles, particularly very small or nanoparticle forms, may persist in tissues and interact with cells in ways that are not fully understood.

Europe Bans Titanium Dioxide in 2022

These concerns prompted a decisive regulatory action in Europe in 2022, when the European Union formally banned titanium dioxide (E171) as a food additive. Following an extensive scientific review, the European Food Safety Authority (EFSA) concluded that titanium dioxide “can no longer be considered safe” for use in food because of unresolved concerns about genotoxicity — the potential to damage DNA. Crucially, EFSA determined that it was not possible to establish a safe daily intake level, meaning regulators could not confidently say that any amount consumed over time was without risk.

As a result, titanium dioxide was removed from foods sold across the EU after a transition period, reflecting a precautionary approach to long-term health protection.

The EU’s decision highlights a growing regulatory divide between Europe and the United States. While Europe moved to eliminate titanium dioxide from foods based on scientific uncertainty alone, U.S. regulators continue to allow its use not only in foods, but also in medications, supplements, and topical products, where exposure may be repeated and cumulative. For consumers, this raises important questions about why an additive deemed unsafe for ingestion in one advanced regulatory system remains commonplace in another — and whether visual appeal should outweigh unresolved concerns about long-term biological effects. The continued presence of titanium dioxide in everyday products underscores the need for greater transparency, updated risk assessments, and a closer examination of whether precautionary principles should play a larger role in U.S. consumer safety standards.

Arsenic

Examples of candies where detectable arsenic was reported in that testing include: 

Black Forest Gummy Bears Laffy Taffy Banana Nerds (grape and strawberry) SweeTarts Trolli Sour Brite Crawlers Jolly Rancher hard candies Twizzlers Kit Kat, 3 Musketeers, Snickers Skittles, Sour Patch Kids, Swedish Fish Tootsie Rolls and fruit chews Some Smart Sweets varieties.

Other Dangerous Ingredients:

Sucrolose

Sucralose (Splenda): Definition, Microbiome Impact, and Where It’s Found

What is Sucralose?

Sucralose is a high-intensity artificial sweetener derived from sugar (sucrose). It is approximately

600 times sweeter than sugar and is widely used to provide sweetness with little to no calories. It is commonly marketed under brand names such as Splenda and is approved for use by regulatory agencies including the FDA.

Primary Health Concern: Impact on the Gut Microbiome

The most consistently cited concern with sucralose is its effect on the gut microbiome. Research suggests that non-nutritive sweeteners may alter the balance and function of gut bacteria, which play a key role in metabolic health, immune regulation, and hormone signaling.

Potential Effects Observed in Studies:

• Changes in gut bacteria composition and activity

• Reduced insulin sensitivity in some individuals after regular exposure

• Impaired glucose tolerance linked to microbiome alterations

These microbiome changes may contribute to blood sugar instability, increased cravings, weight-loss resistance, and inflammation—particularly relevant for individuals with insulin resistance or hormonal transitions such as perimenopause.

Where Sucralose Is Commonly Found (CVS & Walgreens-type Retailers)

Drinks & Beverages

• Diet and zero-sugar sodas

• Sugar-free energy drinks

• Zero-sugar flavored waters

• Ready-to-drink iced teas and coffees labeled “no sugar”

Drink Mixes & Hydration Products

• Zero-sugar electrolyte powders and sticks

• Flavored hydration packets

• Pre-workout and powdered drink enhancers

Protein Bars, Shakes & Powders

• Protein bars marketed as low sugar, keto, or diabetic-friendly

• Ready-to-drink protein shakes

• Flavored protein powders (unflavored versions are less likely)

Supplements

• Gummy vitamins (adult and children’s)

• Chewable supplements (vitamin C, zinc, fiber, melatonin)

• Some liquid and chewable over-the-counter medications

Hygiene & Oral Care Products

• Toothpaste formulations

• Mouthwashes and whitening products

(Sucralose is used to improve taste, not for nutritional value.)

Quick Label-Scanning Tip

Look for “sucralose” in the ingredient list. Products labeled “zero sugar,” “high protein,” “keto,” or

“diet” have a high likelihood of containing it unless otherwise specified.

Bottom Line

While sucralose is permitted by regulatory agencies, growing evidence suggests it may not be biologically neutral—especially with regular, long-term consumption. Its potential impact on gutbacteria and metabolic signaling makes moderation and label awareness especially important.

To wrap it up, the foot traffic and patrons consuming in-store products from beauty, food, beverage, hygiene, and health. Could it be intentional that they are stalking their shelves with medications and products that are driving people to need MORE prescriptions and medications? To have weakened immune systems, mental health issues, brain diseases and cancers?

For the $150 billion per year in profit, the revenue is between 10 and 15% according to sources.The foot traffic and patrons consuming in-store products from beauty, food, beverage, hygiene, and health.

Could it be intentional that they are stocking their shelves with medications and products that are driving people to need MORE prescriptions and medications? To have weakened immune systems, mental health issues, brain diseases and cancers?

Could it be to drive lifelong customers?

Bottom Line. Be Aware. Always Read Ingredients!