Label: BLEACKHEAD REMOVING MEDICATED SCRUB DAYLOGIC- salicylic acid 2.00% lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 11822-7798-4 - Packager: Rite Aid
- 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 May 22, 2018
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
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- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
BLEACKHEAD REMOVING MEDICATED SCRUB DAYLOGIC
salicylic acid 2.00% lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-7798 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 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Cetyl Alcohol (UNII: 936JST6JCN) PPG-15 Stearyl Ether (UNII: 1II18XLS1L) Microcrystalline Wax (UNII: XOF597Q3KY) HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58) Steareth-21 (UNII: 53J3F32P58) Polysorbate 60 (UNII: CAL22UVI4M) Ferric Ferrocyanide (UNII: TLE294X33A) Xanthan Gum (UNII: TTV12P4NEE) Potassium Cetyl Phosphate (UNII: 03KCY6P7UT) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-7798-4 141 g in 1 TUBE; Type 0: Not a Combination Product 09/15/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 09/15/2016 Labeler - Rite Aid (014578892) Registrant - Product Quest Mfg (927768135) Establishment Name Address ID/FEI Business Operations Product Quest Mfg 927768135 manufacture(11822-7798) , label(11822-7798)