Label: CANTU GUAVA GINGER ANTI DANDRUFF- salicylic acid shampoo
- NDC Code(s): 61012-740-13
- Packager: PDC Brands
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 December 28, 2021
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- WARNINGS
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CANTU GUAVA GINGER ANTI DANDRUFF
salicylic acid shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61012-740 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.03 g in 1 mL Inactive Ingredients Ingredient Name Strength BENZOIC ACID (UNII: 8SKN0B0MIM) GLYCERIN (UNII: PDC6A3C0OX) APPLE CIDER VINEGAR (UNII: 0UE22Q87VC) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERETH-2 COCOATE (UNII: JWM00VS7HC) COCO MONOETHANOLAMIDE (UNII: C80684146D) TEA TREE OIL (UNII: VIF565UC2G) PSIDIUM GUAJAVA LEAF (UNII: PM0F263X0Y) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) SODIUM HYDROXIDE (UNII: 55X04QC32I) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) WATER (UNII: 059QF0KO0R) TURMERIC (UNII: 856YO1Z64F) MENTHOL (UNII: L7T10EIP3A) GINGER (UNII: C5529G5JPQ) Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61012-740-13 400 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/28/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 12/28/2021 Labeler - PDC Brands (037512746) Registrant - RNA PHARMA, LLC (079103999) Establishment Name Address ID/FEI Business Operations RNA PHARMA, LLC 079103999 manufacture(61012-740)
