Label: TRIDERMA ACNE GEL FACE WASH- salicylic acid gel
- NDC Code(s): 10738-041-52
- Packager: Genuine Virgin Aloe Corporation
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 2, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
Directions •Use morning and night to cleanse face and body •Pump into your hands and work into lather •Massage lather onto skin with a gentle, circular motion •Avoid direct contact with eyes •If contact occurs, flush thoroughly with water •If bothersome dryness or peeling occurs, reduce application to once a day or every other day •If no discomfort occurs, follow the direction stated above.
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
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SPL UNCLASSIFIED SECTION
For Healthier Looking Skin
Clears acne
Helps prevent new blemishes from forming
• AP4 ® BOTANICAL • ALOE VERA COMPLEX
Maximum Strength Healing Botanicals
Made with acne fighting Salicylic Acid and AP4 ® Organic Aloe* Complex, this clarifying face and body wash gently cleanses skin removing dirt, oil and impurities.
• Clears acne blemishes
• Purifies pores
• Pores look smaller
Dermatologist Tested
No Added Fragrance or Parabens
www.triderma.com
MADE IN THE USA
Dist by:
Genuine Virgin Aloe Corp.
Corona, CA 92879 ©2019
- Packaging
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INGREDIENTS AND APPEARANCE
TRIDERMA ACNE GEL FACE WASH
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10738-041 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM HYDROXIDE (UNII: 55X04QC32I) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALLANTOIN (UNII: 344S277G0Z) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10738-041-52 148 mL in 1 TUBE; Type 0: Not a Combination Product 01/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 01/16/2020 Labeler - Genuine Virgin Aloe Corporation (961374147) Establishment Name Address ID/FEI Business Operations Genuine Virgin Aloe Corporation 961374147 manufacture(10738-041)