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Data / Drug companies / Orazen Inc

Orazen Inc: 26 products in the FDA NDC directory, labeler code 71927

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

Orazen Inc (labeler code 71927) lists 26 products in the FDA National Drug Code Directory, covering 12 finished drugs by generic name. By type: 26 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on September 5, 2026.

The request: Watch Orazen Inc (FDA labeler code 71927): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
71927
Products in commercial distribution
26
Packages
28
Finished drugs by generic name
12
Prescription products
0
Over the counter products
26
Flagged as original packager
26 of 26 products that carry the flag
Started marketing in the last 12 months
7
Earliest marketing start
January 7, 2019
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 drugs26100%

Products by type

TypeProductsShare
Over the counter drugs26100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Cream830.8%
Ointment830.8%
Spray415.4%
Gel311.5%
Liquid13.8%
Kit13.8%
Paste13.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
American Safety and First Aid Triple Antibiotic71927-016OintmentOver the counter monograph drugsSeptember 5, 2026
American Safety and First Aid Triple Antibiotic71927-016OintmentOver the counter monograph drugsSeptember 5, 2026
First Aid Kit, Orazen Inc71927-036KitOver the counter monograph drugsMay 1, 2026
Ora Zen Triple Antibiotic71927-034OintmentOver the counter monograph drugsMarch 11, 2026
Medi first plus71927-033CreamOver the counter monograph drugsDecember 12, 2025
Medi-first71927-032CreamOver the counter monograph drugsDecember 12, 2025
American Safety and First Aid71927-031CreamOver the counter monograph drugsDecember 11, 2025
Medi-first71927-019CreamOver the counter monograph drugsSeptember 3, 2025
Medi-first71927-017OintmentOver the counter monograph drugsSeptember 3, 2025
Medi-first71927-017OintmentOver the counter monograph drugsSeptember 3, 2025
Medi-first71927-019CreamOver the counter monograph drugsAugust 29, 2025
Medi-first71927-017OintmentOver the counter monograph drugsAugust 29, 2025
Circle K Triple Antibiotic71927-022OintmentOver the counter monograph drugsOctober 18, 2023
Lil Drug Store Triple Antibiotic71927-021OintmentOver the counter monograph drugsOctober 18, 2023
Orazen71927-102PasteOver the counter monograph drugsApril 1, 2023
American Safety and First Aid71927-015CreamOver the counter monograph drugsOctober 17, 2022
American Safety and First Aid71927-015CreamOver the counter monograph drugsOctober 17, 2022
American Safety First Aid Antispetic71927-014SprayOver the counter monograph drugsOctober 3, 2022
American Safety First Aid Antispetic71927-013SprayOver the counter monograph drugsOctober 3, 2022
American Safety First Aid71927-012SprayOver the counter monograph drugsOctober 3, 2022
First Aid Antispetic71927-011SprayOver the counter monograph drugsOctober 3, 2022
Medicated Chest Rub71927-020CreamOver the counter monograph drugsFebruary 14, 2022
Hand Sanitizer71927-001GelOver the counter monograph drugsJuly 15, 2020
Hand Sanitizer71927-008GelOver the counter monograph drugsDecember 31, 2019
Mouthwash71927-006LiquidOver the counter monograph drugsApril 22, 2019

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.