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Data / Drug companies / Foundation Consumer Healthcare

Foundation Consumer Healthcare: 20 products in the FDA NDC directory, labeler code 69536

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Foundation Consumer Healthcare (labeler code 69536) lists 20 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 20 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on October 31, 2024.

The request: Watch Foundation Consumer Healthcare (FDA labeler code 69536): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
69536
Products in commercial distribution
20
Packages
31
Finished drugs by generic name
9
Prescription products
0
Over the counter products
20
Flagged as original packager
20 of 20 products that carry the flag
Started marketing in the last 12 months
0
Products with a marketing end date set
1
Earliest marketing start
February 17, 2017
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs1365%
Authorized generics (NDA)315%
New drug applications (NDA)210%
Generic drugs (ANDA)210%

Products by type

TypeProductsShare
Over the counter drugs20100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Tablet525%
Solution420%
Tablet, chewable210%
Gel210%
Kit210%
Tablet, orally disintegrating210%
Tablet, coated15%
Tablet, film coated15%
Liquid15%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Alavert Allergy69536-195Tablet, orally disintegratingGeneric drugs (ANDA)October 31, 2024
Dimetapp Cold and Allergy69536-305SolutionOver the counter monograph drugsJune 15, 2024
Dimetapp Cold and Cough and Dimetapp Nighttime Cold and Cough69536-365KitOver the counter monograph drugsJune 1, 2024
Dimetapp Cold and Cough and Nighttime Cold and Cough69536-355KitOver the counter monograph drugsJune 1, 2024
Dimetapp Nighttime Cold and Cough69536-345SolutionOver the counter monograph drugsJune 1, 2024
Dimetapp Multi-Symptom Cold and Flu69536-335SolutionOver the counter monograph drugsJune 1, 2024
Dimetapp Cold and Cough69536-315SolutionOver the counter monograph drugsJune 1, 2024
Alavert Allergy69536-190Tablet, orally disintegratingGeneric drugs (ANDA)May 1, 2024
Dimetapp Cough and Allergy69536-370Tablet, chewableOver the counter monograph drugsApril 15, 2024
Campho-Phenique Antiseptic69536-109GelOver the counter monograph drugsNovember 15, 2021
Bronkaid Max69536-250Tablet, coatedOver the counter monograph drugsSeptember 1, 2020
Next Choice One Dose69536-133TabletAuthorized generics (NDA)June 15, 2019
Take Action69536-200TabletAuthorized generics (NDA)May 10, 2018
Plan B One-Step69536-162TabletNew drug applications (NDA)May 10, 2018
Plan B One-Step69536-146TabletNew drug applications (NDA)May 10, 2018
Aftera69536-103TabletAuthorized generics (NDA)May 10, 2018
Campho-Phenique Cold Sore Treatment69536-108GelOver the counter monograph drugsAugust 1, 2017
Campho-Phenique Antiseptic69536-110LiquidOver the counter monograph drugsJune 1, 2017
St. Joseph Chewable Low Dose Aspirin69536-281Tablet, chewableOver the counter monograph drugsFebruary 17, 2017
St. Joseph Low Dose Aspirin69536-181Tablet, film coatedOver the counter monograph drugsFebruary 17, 2017

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.