Label: ASPIRE SCRUB SO CLEAN- salicylic acid lotion
-
Contains inactivated NDC Code(s)
NDC Code(s): 60717-310-34 - Packager: RNA PHARMA, LLC
- 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 September 8, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ASPIRE SCRUB SO CLEAN
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60717-310 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PANTHENOL (UNII: WV9CM0O67Z) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) ALOE VERA LEAF (UNII: ZY81Z83H0X) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R) RICE BRAN (UNII: R60QEP13IC) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) EDETATE DISODIUM (UNII: 7FLD91C86K) LEVOMENOL (UNII: 24WE03BX2T) CHAMOMILE (UNII: FGL3685T2X) SORBITOL (UNII: 506T60A25R) CUCUMBER (UNII: YY7C30VXJT) GLYCERIN (UNII: PDC6A3C0OX) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) SODIUM BENZOATE (UNII: OJ245FE5EU) Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60717-310-34 100 mL in 1 TUBE; Type 0: Not a Combination Product 09/08/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 09/08/2021 Labeler - RNA PHARMA, LLC (079103999) Establishment Name Address ID/FEI Business Operations RNA PHARMA, LLC 079103999 manufacture(60717-310)
