Label: NAS MAX STRENGTH SPOT TREATMENT- salicylic acid cream
- NDC Code(s): 26052-022-01
- Packager: BURT'S BEES, INC.
- 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 3, 2018
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- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
- DIRECTIONS
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INACTIVE INGREDIENTS
WATER, CAPRYLIC/CAPRIC TRIGLYCERIDE, GLYCERIN, SALIX NIGRA (WILLOW) BARK EXTRACT, STEARYL ALCOHOL, CETYL ALCOHOL, GLYCERYL STEARATE, BEESWAX, CALOPHYLLUM INOPHYLLUM SEED OIL, CYMBOPOGON SCHOENANTHUS EXTRACT, DIPOTASSIUM GLYCYRRHIZATE, EQUSETUM HIEMALE EXTRACT, HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF EXTRACT, HUMULUS LUPULUS (HOPS) EXTRACT, HYDRASTIS CANADENSIS (GOLDENSEAL) EXTRACT, LONICERA CAPRIFULIUM EXTRACT, LONICERA JAPONICA EXTRACT, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, STEARIC ACID, SORBIC ACID, TOCOPHEROL, XANTHAN GUM, LECITHIN, GLUCOSE, GLYCINE SOJA (SOYBEAN) OIL, FRAGRANCE, SODIUM CHLORIDE, GLUCOSE OXIDASE, LACTOPEROXIDASE, PHENOXYETHANOL.
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INGREDIENTS AND APPEARANCE
NAS MAX STRENGTH SPOT TREATMENT
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:26052-022 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 CYMBOPOGON SCHOENANTHUS TOP (UNII: 9SJI1LW39W) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) PHENOXYETHANOL (UNII: HIE492ZZ3T) TOCOPHEROL (UNII: R0ZB2556P8) SOYBEAN OIL (UNII: 241ATL177A) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) SALIX NIGRA BARK (UNII: QU52J3A5B3) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CETYL ALCOHOL (UNII: 936JST6JCN) WHITE WAX (UNII: 7G1J5DA97F) TAMANU OIL (UNII: JT3LVK84A1) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV) STEARIC ACID (UNII: 4ELV7Z65AP) HUMULUS LUPULUS WHOLE (UNII: 912A6Q1N4A) HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T) LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) GLUCOSE OXIDASE (UNII: 0T8392U5N1) LACTOPEROXIDASE BOVINE (UNII: 01UIN5OC49) XANTHAN GUM (UNII: TTV12P4NEE) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) POTASSIUM STEARATE (UNII: 17V812XK50) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:26052-022-01 1 in 1 CARTON 11/01/2011 1 10 g 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 11/01/2011 Labeler - BURT'S BEES, INC. (613480946)
