NDC 72073-003 Renardblanc Acne Cleansing Bar
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 72073-003?
What are the uses for Renardblanc Acne Cleansing Bar?
Which are Renardblanc Acne Cleansing Bar 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 Renardblanc Acne Cleansing Bar 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:
- SODIUM PALMATE (UNII: S0A6004K3Z)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)
- STARCH, CORN (UNII: O8232NY3SJ)
- COCAMIDOPROPYL DIMETHYLAMINE (UNII: L36BM7DG2T)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- COCONUT OIL (UNII: Q9L0O73W7L)
- HYDROGENATED JOJOBA OIL (UNII: 7F674YQ5SO)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- HYALURONIC ACID (UNII: S270N0TRQY)
- ALLANTOIN (UNII: 344S277G0Z)
What is the NDC to RxNorm Crosswalk for Renardblanc Acne Cleansing Bar?
- RxCUI: 2047180 - salicylic acid 0.6 % Medicated Bar Soap
- RxCUI: 2047180 - salicylic acid 0.006 MG/MG Medicated Bar Soap
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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".