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Data / Drug companies / Abbe Laboratories, Inc.

Abbe Laboratories, Inc.: 7 products in the FDA NDC directory, labeler code 68605

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

Abbe Laboratories, Inc. (labeler code 68605) lists 7 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 7 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on May 1, 2022.

The request: Watch Abbe Laboratories, Inc. (FDA labeler code 68605): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
68605
Products in commercial distribution
7
Packages
17
Finished drugs by generic name
5
Prescription products
0
Over the counter products
7
Flagged as original packager
4 of 4 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
April 20, 2004
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 drugs7100%

Products by type

TypeProductsShare
Over the counter drugs7100%

Drugs it lists

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

DrugProductsCompanies listing it
Sulfur252
Benzethonium chloride227
Diaper rash ointment11
Petrolatum and lanolin11
Meradimate, octinoxate, octisalate, oxybenzone12

Dosage forms

Dosage formProductsShare
Lotion, augmented228.6%
Ointment228.6%
Gel228.6%
Lotion114.3%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Pro-Tect Sports Sunscreen SPF 2068605-8640LotionOver the counter monograph drugsMay 1, 2022
A-Cute Derm Antisepation68605-7171GelOver the counter monograph drugsMay 1, 2022
A-Cute Derm B-Kleer68605-1040GelOver the counter monograph drugsMay 1, 2022
Grandma Els68605-2007OintmentOver the counter monograph drugsFebruary 1, 2015
Veradex-e68605-3700OintmentOver the counter monograph drugsJanuary 1, 2008
End-zit68605-2002Lotion, augmentedOver the counter monograph drugsApril 20, 2004
End-zit68605-2001Lotion, augmentedOver the counter monograph drugsApril 20, 2004

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.