NDC 70381-111 Acne Control Acne Body Wash
View Dosage, Usage, Ingredients, Routes, UNII
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Product Characteristics
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Product Details
What is NDC 70381-111?
What are the uses for Acne Control Acne Body Wash?
Which are Acne Control Acne Body Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Acne Control Acne Body Wash Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C)
- PEG-200 HYDROGENATED GLYCERYL PALMATE (UNII: W161T051Y1)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- TOCOPHEROL (UNII: R0ZB2556P8)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- PHOENIX DACTYLIFERA SEED (UNII: 73NE6T0Q00)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- POLIGLUSAM (UNII: 82LKS4QV2Y)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- UREA (UNII: 8W8T17847W)
- AMINO ACIDS, SOURCE UNSPECIFIED (UNII: 0O72R8RF8A)
- TREHALOSE (UNII: B8WCK70T7I)
- INOSITOL (UNII: 4L6452S749)
- TAURINE (UNII: 1EQV5MLY3D)
- BETAINE (UNII: 3SCV180C9W)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- PROPANEDIOL (UNII: 5965N8W85T)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- SODIUM BISULFITE (UNII: TZX5469Z6I)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
What is the NDC to RxNorm Crosswalk for Acne Control Acne Body Wash?
- RxCUI: 1038982 - salicylic acid 1 % Medicated Liquid Soap
- RxCUI: 1038982 - salicylic acid 10 MG/ML Medicated Liquid Soap
* Please review the disclaimer below.
Patient Education
Salicylic Acid Topical
Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions that involve scaling or overgrowth of skin cells such as psoriasis (a skin disease in which red, scaly patches form on some areas of the body), ichthyoses (inborn conditions that cause skin dryness and scaling), dandruff, corns, calluses, and warts on the hands or feet. Topical salicylic acid should not be used to treat genital warts, warts on the face, warts with hair growing from them, warts in the nose or mouth, moles, or birthmarks. Salicylic acid is in a class of medications called keratolytic agents. Topical salicylic acid treats acne by reducing swelling and redness and unplugging blocked skin pores to allow pimples to shrink. It treats other skin conditions by softening and loosening dry, scaly, or thickened skin so that it falls off or can be removed easily.
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* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".