NDC 11822-8200 Renewal
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 11822-8200?
What are the uses for Renewal?
Which are Renewal 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 Renewal 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 C14 OLEFIN SULFONATE (UNII: N816E2SOKI)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CHAMOMILE (UNII: FGL3685T2X)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
What is the NDC to RxNorm Crosswalk for Renewal?
- RxCUI: 317152 - salicylic acid 2 % Topical Cream
- RxCUI: 317152 - salicylic acid 20 MG/ML Topical Cream
* 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".