NDC 42783-635 Advanced Acne Wash
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 42783-635?
What are the uses for Advanced Acne Wash?
Which are Advanced Acne Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- DOXYCYCLINE (UNII: N12000U13O)
- DOXYCYCLINE ANHYDROUS (UNII: 334895S862) (Active Moiety)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Advanced Acne 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- TALC (UNII: 7SEV7J4R1U)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SHEA BUTTER (UNII: K49155WL9Y)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CANDELILLA WAX (UNII: WL0328HX19)
- HYDROXYETHYL BEHENAMIDOPROPYL DIMONIUM CHLORIDE (UNII: 9CO8OUL4TH)
- LAURETH-7 (UNII: Z95S6G8201)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Advanced Acne Wash?
- RxCUI: 1543390 - benzoyl peroxide 4.4 % Medicated Liquid Soap
- RxCUI: 1543390 - benzoyl peroxide 44 MG/ML Medicated Liquid Soap
- RxCUI: 1650142 - doxycycline monohydrate 100 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Benzoyl Peroxide Topical
Benzoyl peroxide is used to treat mild to moderate acne.
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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".