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Data / Drug companies / Wakefern Food Corp.

Wakefern Food Corp.: 5 products in the FDA NDC directory, labeler code 41190

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

Wakefern Food Corp. (labeler code 41190) lists 5 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 5 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on May 6, 2024.

The request: Watch Wakefern Food Corp. (FDA labeler code 41190): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
41190
Products in commercial distribution
5
Packages
7
Finished drugs by generic name
3
Prescription products
0
Over the counter products
5
Flagged as original packager
5 of 5 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
January 27, 2015
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 drugs5100%

Products by type

TypeProductsShare
Over the counter drugs5100%

Drugs it lists

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

DrugProductsCompanies listing it
Alcohol3293
Benzalkonium chloride 0.13%119
Petrolatum174

Dosage forms

Dosage formProductsShare
Gel240%
Soap120%
Liquid120%
Ointment120%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Skin Protectant41190-180OintmentOver the counter monograph drugsMay 6, 2024
Alcohol41190-849LiquidOver the counter monograph drugsJune 21, 2022
Benzalkonium chloride41190-278SoapOver the counter monograph drugsJuly 10, 2017
Advanced Hand Sanitizer41190-439GelOver the counter monograph drugsFebruary 3, 2015
Advanced Hand Sanitizer41190-370GelOver the counter monograph drugsJanuary 27, 2015

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.