NDC 11822-8210 Rite Aid Renewal
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 11822-8210?
What are the uses for Rite Aid Renewal?
Which are Rite Aid 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 Rite Aid 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)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARETH-15 (UNII: O6V041E38J)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- STEARETH-21 (UNII: 53J3F32P58)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- NEOPENTYL GLYCOL DICAPRATE (UNII: 77T908SE82)
- COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- AGAR (UNII: 89T13OHQ2B)
- MENTHOL (UNII: L7T10EIP3A)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Rite Aid Renewal?
- RxCUI: 317152 - salicylic acid 2 % Topical Cream
- RxCUI: 317152 - salicylic acid 20 MG/ML Topical Cream
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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".