NDC 72934-1129

IMIQUIMOD 5% / TRETINOIN 0.025%

Imiquimod 5% / Tretinoin 0.025%

IMIQUIMOD 5% / TRETINOIN 0.025% is a Topical Gel in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Tretinoin; Imiquimod.

• Product ID: 72934-1129_8839ed49-b52b-11f6-e053-2a95a90a7492
• NDC: 72934-1129
• Product Type: Human Prescription Drug
• Proprietary Name: IMIQUIMOD 5% / TRETINOIN 0.025%
• Generic Name: Imiquimod 5% / Tretinoin 0.025%
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-05-07
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Sincerus Florida, LLC
• Substance Name: TRETINOIN; IMIQUIMOD
• Active Ingredient Strength: 0 g/100g; g/100g
• Pharm Classes: Retinoid [EPC],Retinoids [CS],Increased Cytokine Activity [PE],Increased Cytokine Production [PE],Interferon Inducers [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 72934-1129-2

30 g in 1 BOTTLE, PUMP (72934-1129-2)

• Marketing Start Date: 2019-05-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72934-1129-2 [72934112902]

IMIQUIMOD 5% / TRETINOIN 0.025% GEL

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-05-07

Drug Details

Active Ingredients

Ingredient	Strength
TRETINOIN	.025 g/100g

Pharmacological Class

• Retinoid [EPC]
• Retinoids [CS]
• Increased Cytokine Activity [PE]
• Increased Cytokine Production [PE]
• Interferon Inducers [MoA]
• Retinoid [EPC]
• Retinoids [CS]
• Increased Cytokine Activity [PE]
• Increased Cytokine Production [PE]
• Interferon Inducers [MoA]