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Data / Drug companies / KW Absc, Inc.

KW Absc, Inc.: 14 products in the FDA NDC directory, labeler code 69231

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

KW Absc, Inc. (labeler code 69231) lists 14 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 14 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on November 9, 2022.

The request: Watch KW Absc, Inc. (FDA labeler code 69231): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
69231
Products in commercial distribution
14
Packages
14
Finished drugs by generic name
2
Prescription products
0
Over the counter products
14
Flagged as original packager
14 of 14 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
November 23, 2018
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 drugs14100%

Products by type

TypeProductsShare
Over the counter drugs14100%

Drugs it lists

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

DrugProductsCompanies listing it
Titanium dioxide, octinoxate, octisalate122
Titanium dioxide, octinoxate, octisalate, avobenzone21

Dosage forms

Dosage formProductsShare
Cream14100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
CLE CCC Neutral Deep69231-036CreamOver the counter monograph drugsNovember 9, 2022
CLE CCC Warm Deep69231-032CreamOver the counter monograph drugsNovember 8, 2022
CLE CCC Olive Medium Deep69231-035CreamOver the counter monograph drugsOctober 25, 2022
CLE CCC Golden Medium69231-034CreamOver the counter monograph drugsOctober 25, 2022
CLE CCC Neutral Fair69231-033CreamOver the counter monograph drugsOctober 24, 2022
CLE CCC Cool Medium Deep69231-031CreamOver the counter monograph drugsOctober 24, 2022
CLE CCC Neutral Medium69231-030CreamOver the counter monograph drugsOctober 18, 2022
CLE CCC Neutral Medium Light69231-029CreamOver the counter monograph drugsOctober 18, 2022
CLE CCC Neutral Light69231-028CreamOver the counter monograph drugsOctober 18, 2022
CLE CCC Golden Medium Deep69231-027CreamOver the counter monograph drugsDecember 3, 2018
CLE CCC Warm Medium Deep69231-026CreamOver the counter monograph drugsNovember 29, 2018
CLE CCC Warm Medium69231-025CreamOver the counter monograph drugsNovember 27, 2018
CLE CCC Warm Medium Light69231-024CreamOver the counter monograph drugsNovember 27, 2018
CLE CCC Warm Light69231-023CreamOver the counter monograph drugsNovember 23, 2018

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.