NDC 21839-680 Natures Cure Body Acne Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 21839-680?
What are the uses for Natures Cure Body Acne Treatment?
Which are Natures Cure Body Acne Treatment 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 Natures Cure Body Acne Treatment 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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- CINNAMON BARK OIL (UNII: XE54U569EC)
- CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- WATER (UNII: 059QF0KO0R)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- SALIX NIGRA BARK (UNII: QU52J3A5B3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- TROLAMINE (UNII: 9O3K93S3TK)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALCOHOL (UNII: 3K9958V90M)
- SARCOSINE (UNII: Z711V88R5F)
- CHAMOMILE (UNII: FGL3685T2X)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALLANTOIN (UNII: 344S277G0Z)
What is the NDC to RxNorm Crosswalk for Natures Cure Body Acne Treatment?
- RxCUI: 1048903 - salicylic acid 2 % Topical Spray
- RxCUI: 1048903 - salicylic acid 20 MG/ML Topical Spray
* 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".