NDC 65903-247 Anti Acne Clarifying Face Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65903 - H2o Plus
- 65903-247 - Anti Acne Clarifying Face Wash
Product Packages
NDC Code 65903-247-01
Package Description: 118 mL in 1 TUBE
Product Details
What is NDC 65903-247?
What are the uses for Anti Acne Clarifying Face Wash?
Which are Anti Acne Clarifying Face 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 Anti Acne Clarifying Face 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 C12-14 OLEFIN SULFONATE (UNII: 7I962MCQ71)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- MENTHOL (UNII: L7T10EIP3A)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)
- CHINESE CINNAMON (UNII: WS4CQ062KM)
- GINGER (UNII: C5529G5JPQ)
- CRITHMUM MARITIMUM (UNII: J7IHY79BKY)
- HIMANTHALIA ELONGATA (UNII: 21RND18XRR)
- MASTOCARPUS STELLATUS (UNII: 6T087FC66H)
- MACROCYSTIS PYRIFERA (UNII: K31S3OG5C4)
What is the NDC to RxNorm Crosswalk for Anti Acne Clarifying Face Wash?
- RxCUI: 416212 - salicylic acid 1.5 % Topical Gel
- RxCUI: 416212 - salicylic acid 0.015 MG/MG Topical Gel
* 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".