Label: POST TREATMENT BALM- hydrocortisone cream
- NDC Code(s): 62742-4077-1, 62742-4077-2
- Packager: Allure Labs Inc.
- 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 December 3, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive Ingredients:
Petrolatum, Carthamus Tinctorius (Safflower) Seed Oil, Tocopheryl Acetate, Zinc Oxide , Titanium Dioxide, Caprylic/Capric Triglyceride, Glyceryl Isostearate, Polyhydroxystearic Acid , Glycosaminoglycans, Dimethicone, Triethoxycaprylylsilane, PEG-8 , Tocopherol , Ascorbyl Palmitate , Ascorbic Acid, Citric Acid
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
POST TREATMENT BALM
hydrocortisone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4077 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 1 mg in 1 g Inactive Ingredients Ingredient Name Strength LECITHIN, SOYBEAN (UNII: 1DI56QDM62) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) GAG (UNII: U5T7CTT5KM) ASCORBYL PALMITATE (UNII: QN83US2B0N) ASCORBIC ACID (UNII: PQ6CK8PD0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SAFFLOWER (UNII: 4VBL71TY4Y) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) ACETATE ION (UNII: 569DQM74SC) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) ISOSTEARIC ACID (UNII: X33R8U0062) TOCOPHEROL (UNII: R0ZB2556P8) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) HEXYLENE GLYCOL (UNII: KEH0A3F75J) PETROLATUM (UNII: 4T6H12BN9U) SAFFLOWER OIL (UNII: 65UEH262IS) ZINC OXIDE (UNII: SOI2LOH54Z) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4077-2 29.6 g in 1 TUBE; Type 0: Not a Combination Product 05/12/2015 2 NDC:62742-4077-1 56.7 g in 1 TUBE; Type 0: Not a Combination Product 05/12/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 05/12/2015 Labeler - Allure Labs Inc. (926831603) Registrant - Allure Labs (926831603) Establishment Name Address ID/FEI Business Operations Allure Labs 926831603 manufacture(62742-4077)