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Data / Drug companies / Camber Consumer Care Inc

Camber Consumer Care Inc: 30 products in the FDA NDC directory, labeler code 69230

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

Camber Consumer Care Inc (labeler code 69230) lists 30 products in the FDA National Drug Code Directory, covering 15 finished drugs by generic name. By type: 24 over the counter drugs, 6 drugs for further processing. Its main marketing category is generic drugs (ANDA). The newest product started marketing on September 30, 2025.

The request: Watch Camber Consumer Care Inc (FDA labeler code 69230): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
69230
Products in commercial distribution
30
Packages
95
Finished drugs by generic name
15
Prescription products
0
Over the counter products
24
Flagged as original packager
24 of 24 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
September 16, 2015
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)2273.3%
Drugs for further processing620%
Over the counter monograph drugs26.7%

Products by type

TypeProductsShare
Over the counter drugs2480%
Drugs for further processing620%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet1033.3%
Tablet, film coated930%
Suspension413.3%
Solution413.3%
Capsule, delayed release13.3%
Powder, for solution13.3%
Tablet, delayed release13.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Levonorgestrel69230-333TabletGeneric drugs (ANDA)September 30, 2025
Adult Tussin69230-332SolutionOver the counter monograph drugsMay 19, 2025
Day time high blood pressure cold and flu69230-331SolutionOver the counter monograph drugsJanuary 1, 2025
Loratadine69230-323TabletDrugs for further processingJuly 28, 2023
Loratadine69230-323TabletGeneric drugs (ANDA)July 28, 2023
Naproxen sodium69230-329Tablet, film coatedGeneric drugs (ANDA)October 28, 2022
Loratadine69230-328TabletGeneric drugs (ANDA)July 31, 2022
Fexofenadine HCl69230-201Tablet, film coatedGeneric drugs (ANDA)December 8, 2021
Famotidine69230-327Tablet, film coatedDrugs for further processingNovember 8, 2021
Famotidine69230-327Tablet, film coatedGeneric drugs (ANDA)November 8, 2021
Famotidine69230-326Tablet, film coatedDrugs for further processingNovember 8, 2021
Famotidine69230-326Tablet, film coatedGeneric drugs (ANDA)November 8, 2021
Loperamide Hydrochloride and Simethicone69230-325TabletGeneric drugs (ANDA)June 17, 2021
Loperamide hydrochloride and simethicone69230-325TabletDrugs for further processingJune 17, 2021
Loratadine69230-322SolutionGeneric drugs (ANDA)May 7, 2021
Polyethylene Glycol 335069230-324Powder, for solutionGeneric drugs (ANDA)April 14, 2021
Levocetirizine dihydrochloride69230-321Tablet, film coatedDrugs for further processingOctober 28, 2020
Levocetirizine Dihydrochloride69230-321Tablet, film coatedGeneric drugs (ANDA)October 28, 2020
Esomeprazole Magnesium69230-320Capsule, delayed releaseGeneric drugs (ANDA)June 2, 2020
Omeprazole69230-318Tablet, delayed releaseGeneric drugs (ANDA)March 25, 2020
Ibuprofen Oral69230-311SuspensionGeneric drugs (ANDA)September 18, 2019
Ibuprofen Oral69230-310SuspensionGeneric drugs (ANDA)September 18, 2019
Ibuprofen Oral69230-309SuspensionGeneric drugs (ANDA)September 18, 2019
Childrens allergy relief69230-316SolutionGeneric drugs (ANDA)March 13, 2019
Allergy Relief69230-304TabletGeneric drugs (ANDA)December 31, 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.