NDC 72934-2163

NIACINAMIDE 4% / TRETINOIN 0.05%

Niacinamide 4% / Tretinoin 0.05%

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

Product ID72934-2163_87386316-d023-a7a9-e053-2991aa0a72cb
NDC72934-2163
Product TypeHuman Prescription Drug
Proprietary NameNIACINAMIDE 4% / TRETINOIN 0.05%
Generic NameNiacinamide 4% / Tretinoin 0.05%
Dosage FormCream
Route of AdministrationTOPICAL
Marketing Start Date2019-05-01
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 72934-2163-2

30 g in 1 BOTTLE, PUMP (72934-2163-2)
Marketing Start Date2019-05-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 72934-2163-2 [72934216302]

NIACINAMIDE 4% / TRETINOIN 0.05% CREAM
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date2019-05-01

NDC 72934-2163-4 [72934216304]

NIACINAMIDE 4% / TRETINOIN 0.05% CREAM
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-07

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%

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