NDC 72934-1165

NIACINAMIDE 4% / TRETINOIN 0.1%

Niacinamide 4% / Tretinoin 0.1%

NIACINAMIDE 4% / TRETINOIN 0.1% 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 ID: 72934-1165_852c07b2-5275-28b0-e053-2a91aa0a4e70
• NDC: 72934-1165
• Product Type: Human Prescription Drug
• Proprietary Name: NIACINAMIDE 4% / TRETINOIN 0.1%
• Generic Name: Niacinamide 4% / Tretinoin 0.1%
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-05-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Sincerus Florida, LLC
• Substance Name: TRETINOIN; NIACINAMIDE
• Active Ingredient Strength: 0 g/100g; g/100g
• Pharm Classes: Retinoid [EPC],Retinoids [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 72934-1165-2

30 g in 1 BOTTLE, PUMP (72934-1165-2)

• Marketing Start Date: 2019-05-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72934-1165-2 [72934116502]

NIACINAMIDE 4% / TRETINOIN 0.1% GEL

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-05-01

Drug Details

Active Ingredients

Ingredient	Strength
TRETINOIN	.1 g/100g

Pharmacological Class

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

NDC Crossover Matching brand name "NIACINAMIDE 4% / TRETINOIN 0.1%" or generic name "Niacinamide 4% / Tretinoin 0.1%"

NDC	Brand Name	Generic Name
72934-1165	NIACINAMIDE 4% / TRETINOIN 0.1%	NIACINAMIDE 4% / TRETINOIN 0.1%
72934-2168	NIACINAMIDE 4% / TRETINOIN 0.1%	NIACINAMIDE 4% / TRETINOIN 0.1%