Label: TRETINOIN gel

  • NDC Code(s): 21922-056-04, 21922-056-06, 21922-057-04, 21922-057-06
  • Packager: Encube Ethicals Private Limited
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated March 4, 2025

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  • DESCRIPTION
    Tretinoin Gel, USP is used for the topical treatment of acne vulgaris. Tretinoin Gel, USP contains tretinoin (retinoic acid, vitamin A acid) in either of two strengths, 0.025% or 0.01% by weight ...
  • CLINICAL PHARMACOLOGY
    Although the exact mode of action of tretinoin is unknown, current evidence suggests that topical tretinoin decreases cohesiveness of follicular epithelial cells with decreased microcomedo ...
  • INDICATIONS AND USAGE
    Tretinoin gel is indicated for topical application in the treatment of acne vulgaris. The safety and efficacy of the long-term use of this product in the treatment of other disorders have not been ...
  • CONTRAINDICATIONS
    Use of the product should be discontinued if hypersensitivity to any of the ingredients is noted.
  • WARNINGS
    GELS ARE FLAMMABLE. AVOID FIRE, FLAME OR SMOKING DURING USE. Keep out of reach of children. Keep tube tightly closed. Do not expose to heat or store at temperatures above 120°F (49°C).
  • PRECAUTIONS
    General - If a reaction suggesting sensitivity or chemical irritation occurs, use of the medication should be discontinued. Exposure to sunlight, including sunlamps, should be minimized during ...
  • ADVERSE REACTIONS
    The skin of certain sensitive individuals may become excessively red, edematous, blistered, or crusted. If these effects occur, the medication should either be discontinued until the integrity of ...
  • OVERDOSAGE
    If medication is applied excessively, no more rapid or better results will be obtained and marked redness, peeling, or discomfort may occur. Oral ingestion of the drug may lead to the same side ...
  • DOSAGE AND ADMINISTRATION
    Tretinoin Gel, USP should be applied once a day, before retiring, to the skin where acne lesions appear, using enough to cover the entire affected area lightly. Gel: Excessive application results ...
  • HOW SUPPLIED
    Tretinoin Gel, USP is supplied as: NDC Code  Strength - Quantity  - 21922-056-04 - 0.01% 15 g - 21922-056-06 - 0.01% 45 g - 21922-057-04 0.025% 15 g - 21922-057-06 0.025% 45 ...
  • SPL PATIENT PACKAGE INSERT
    PATIENT INSTRUCTIONS -   TRETINOIN GEL - For Topical Use Only - Acne Treatment -  IMPORTANT - Read Directions Carefully Before Using -   THIS LEAFLET TELLS YOU ABOUT TRETINOIN GEL ...
  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
    Carton Label - 15 g - NDC 21922-056-04 - Tretinoin Gel, USP 0.01% For Topical Use Only - Net Wt. 15 g - Rx only -      Carton Label - 45 g - NDC 21922-056-06 - Tretinoin Gel, USP ...
  • INGREDIENTS AND APPEARANCE
    Product Information