NDC 72934-1164

NIACINAMIDE 4% / TRETINOIN 0.05%

Niacinamide 4% / Tretinoin 0.05%

NIACINAMIDE 4% / TRETINOIN 0.05% is a Topical Gel in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Tretinoin; Niacinamide.

Product ID72934-1164_87fde6db-944e-e50d-e053-2a95a90a52a4
NDC72934-1164
Product TypeHuman Prescription Drug
Proprietary NameNIACINAMIDE 4% / TRETINOIN 0.05%
Generic NameNiacinamide 4% / Tretinoin 0.05%
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2019-05-04
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameSincerus Florida, LLC
Substance NameTRETINOIN; NIACINAMIDE
Active Ingredient Strength0 g/100g; g/100g
Pharm ClassesRetinoid [EPC],Retinoids [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 72934-1164-2

30 g in 1 BOTTLE, PUMP (72934-1164-2)
Marketing Start Date2019-05-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 72934-1164-2 [72934116402]

NIACINAMIDE 4% / TRETINOIN 0.05% GEL
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-04

Drug Details

Active Ingredients

IngredientStrength
TRETINOIN.05 g/100g

Pharmacological Class

  • Retinoid [EPC]
  • Retinoids [CS]
  • Retinoid [EPC]
  • Retinoids [CS]

NDC Crossover Matching brand name "NIACINAMIDE 4% / TRETINOIN 0.05%" or generic name "Niacinamide 4% / Tretinoin 0.05%"

NDCBrand NameGeneric Name
72934-1163NIACINAMIDE 4% / TRETINOIN 0.05%NIACINAMIDE 4% / TRETINOIN 0.05%
72934-1164NIACINAMIDE 4% / TRETINOIN 0.05%NIACINAMIDE 4% / TRETINOIN 0.05%
72934-2163NIACINAMIDE 4% / TRETINOIN 0.05%NIACINAMIDE 4% / TRETINOIN 0.05%
72934-2168NIACINAMIDE 4% / TRETINOIN 0.05%NIACINAMIDE 4% / TRETINOIN 0.05%

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.