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Data / Drug companies / Bioelements, Inc.

Bioelements, Inc.: 5 products in the FDA NDC directory, labeler code 49825

Bioelements, Inc. (labeler code 49825) 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 September 1, 2024.

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Labeler code
49825
Products in commercial distribution
5
Packages
6
Finished drugs by generic name
3
Prescription products
0
Over the counter products
5
Flagged as original packager
2 of 2 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
April 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
Sulfur152
Sulfur, resorcinol12
Salicylic acid1330

Dosage forms

Dosage formProductsShare
Lotion240%
Cream240%
Paste120%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Spot Defy49825-200LotionOver the counter monograph drugsSeptember 1, 2024
Stage Fight Acne Mask49825-137PasteOver the counter monograph drugsSeptember 1, 2024
Daily Meds49825-100LotionOver the counter monograph drugsSeptember 1, 2024
SPF 50 Face Sunscreen Bioelements49825-201CreamOver the counter monograph drugsJanuary 4, 2016
Ray Defense Broad Spectrum SPF 3049825-138CreamOver the counter monograph drugsApril 27, 2015

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