NDC 71447-009 Nelly Devuyst Serum Bioacne
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 71447-009?
What are the uses for Nelly Devuyst Serum Bioacne?
Which are Nelly Devuyst Serum Bioacne 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 Nelly Devuyst Serum Bioacne 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:
- LEVULINIC ACID (UNII: RYX5QG61EI)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PROPANEDIOL (UNII: 5965N8W85T)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
- WATER (UNII: 059QF0KO0R)
- THYMUS VULGARIS LEAF (UNII: GRX3499643)
- LAVANDIN OIL (UNII: 9RES347CKG)
- ALCOHOL (UNII: 3K9958V90M)
- LIME OIL (UNII: UZH29XGA8G)
- CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
- ARGININE (UNII: 94ZLA3W45F)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- TEA TREE OIL (UNII: VIF565UC2G)
- SILVER CITRATE (UNII: CKA421A1J7)
- MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974)
- MICHELIA ALBA LEAF OIL (UNII: 002RK9L1FN)
What is the NDC to RxNorm Crosswalk for Nelly Devuyst Serum Bioacne?
- RxCUI: 251577 - salicylic acid 2 % Topical Solution
- RxCUI: 251577 - salicylic acid 20 MG/ML Topical Solution
* 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".