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Data / Drug companies / Premier Brands of America Inc.

Premier Brands of America Inc.: 32 products in the FDA NDC directory, labeler code 56104

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

Premier Brands of America Inc. (labeler code 56104) lists 32 products in the FDA National Drug Code Directory, covering 21 finished drugs by generic name. By type: 32 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on September 4, 2026.

The request: Watch Premier Brands of America Inc. (FDA labeler code 56104): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
56104
Products in commercial distribution
32
Packages
33
Finished drugs by generic name
21
Prescription products
0
Over the counter products
32
Flagged as original packager
26 of 26 products that carry the flag
Started marketing in the last 12 months
5
Products with a marketing end date set
3
Earliest marketing start
January 1, 2013
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 drugs32100%

Products by type

TypeProductsShare
Over the counter drugs32100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Aerosol, spray1031.2%
Patch825%
Liquid618.8%
Powder412.5%
Aerosol, powder26.2%
Spray13.1%
Gel13.1%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Jock Itch Powder56104-122PowderOver the counter monograph drugsSeptember 4, 2026
Burn Relief56104-914Aerosol, sprayOver the counter monograph drugsJuly 17, 2026
Athletes Foot56104-912Aerosol, powderOver the counter monograph drugsMay 26, 2026
Medicated Callus Removers56104-913PatchOver the counter monograph drugsMay 22, 2026
Premier Solutions Wart Removers56104-911PatchOver the counter monograph drugsMay 8, 2026
Foot and Leg Pain Relief56104-007Aerosol, sprayOver the counter monograph drugsOctober 8, 2025
Miconazole Nitrate56104-907Aerosol, powderOver the counter monograph drugsJune 27, 2025
Salicylic Acid56104-905PatchOver the counter monograph drugsJune 26, 2025
Medicated Athletes Foot Powder56104-906PowderOver the counter monograph drugsJune 24, 2025
Miconazole nitrate56104-903Aerosol, sprayOver the counter monograph drugsJune 18, 2025
Calamine Plus Pramoxine HCl56104-100Aerosol, sprayOver the counter monograph drugsMay 28, 2025
Antifungal Liquid56104-902LiquidOver the counter monograph drugsNovember 6, 2024
Anti-fungal Powder Miconazole Nitrate56104-500PowderOver the counter monograph drugsSeptember 12, 2023
Liquid Bandage56104-502LiquidOver the counter monograph drugsSeptember 11, 2023
Liquid Callus Remover56104-501LiquidOver the counter monograph drugsSeptember 11, 2023
Witch Hazel56104-904SprayOver the counter monograph drugsAugust 27, 2023
Premier Solutions Antifungal Tolnaftate Liquid56104-247Aerosol, sprayOver the counter monograph drugsJune 16, 2022
Premier Solutions Liquid Bandage56104-246LiquidOver the counter monograph drugsJune 16, 2022
Liquid Wart Remover56104-245LiquidOver the counter monograph drugsJune 16, 2022
Premier Solutions Liquid Corn and Callus Remover56104-255LiquidOver the counter monograph drugsJune 15, 2022
Miconazole Nitrate56104-121Aerosol, sprayOver the counter monograph drugsApril 12, 2022
Anti- Fungal Miconazole Nitrate56104-253PowderOver the counter monograph drugsApril 11, 2022
Salicylic Acid56104-910PatchOver the counter monograph drugsFebruary 22, 2022
Salicylic Acid56104-258PatchOver the counter monograph drugsFebruary 22, 2022
Calamine Plus Pramoxine HCl56104-251Aerosol, sprayOver the counter monograph drugsDecember 20, 2021

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.