NDC 51439-006 Tonic Acne Clearing Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51439 - Carepluss Pharma S.a. De C.v.
- 51439-006 - Tonic
Product Packages
NDC Code 51439-006-01
Package Description: .12 mg in 1 BOTTLE
Product Details
What is NDC 51439-006?
What are the uses for Tonic Acne Clearing Treatment?
Which are Tonic Acne Clearing 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 Tonic Acne Clearing 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:
- DODECYLBENZENESULFONIC ACID (UNII: 60NSK897G9)
- ALCOHOL (UNII: 3K9958V90M)
- HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ETHYLENE GLYCOL (UNII: FC72KVT52F)
- VITAMIN A (UNII: 81G40H8B0T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- EDETIC ACID (UNII: 9G34HU7RV0)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Tonic Acne Clearing Treatment?
- RxCUI: 251577 - salicylic acid 2 % Topical Solution
- RxCUI: 251577 - salicylic acid 20 MG/ML Topical Solution
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[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".