Label: ASPIRE TREAT SO DEEP- salicylic acid gel
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Contains inactivated NDC Code(s)
NDC Code(s): 60717-312-05 - 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 9, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ASPIRE TREAT SO DEEP
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60717-312 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM CITRATE (UNII: 1Q73Q2JULR) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CAPRYLYL GLYCOL (UNII: 00YIU5438U) OLEANOLIC ACID (UNII: 6SMK8R7TGJ) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) ALCOHOL (UNII: 3K9958V90M) LEVOMENOL (UNII: 24WE03BX2T) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) SODIUM HYDROXIDE (UNII: 55X04QC32I) PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6) SACCHARIDE ISOMERATE (UNII: W8K377W98I) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PEG-60 ALMOND GLYCERIDES (UNII: 4Y0E651N0F) ALLANTOIN (UNII: 344S277G0Z) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) NORDIHYDROGUAIARETIC ACID, (+/-)- (UNII: 7PZ73W4ZNR) Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60717-312-05 1 in 1 BOX 09/09/2021 1 15 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 09/09/2021 Labeler - RNA PHARMA, LLC (079103999) Establishment Name Address ID/FEI Business Operations RNA PHARMA, LLC 079103999 manufacture(60717-312)
