NDC 58826-702 Coats Aloe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 58826-702?
What are the uses for Coats Aloe?
Which are Coats Aloe UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Coats Aloe 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:
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BOROGLYCERIN (UNII: U3LMU4AN21)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- DIETHYLHEXYL ADIPATE (UNII: MBY1SL921L)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- TOCOPHEROL (UNII: R0ZB2556P8)
- LAURETH-4 (UNII: 6HQ855798J)
- LAURETH-23 (UNII: N72LMW566G)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- WATER (UNII: 059QF0KO0R)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Coats Aloe?
- RxCUI: 1087954 - allantoin 0.5 % Topical Lotion
- RxCUI: 1087954 - allantoin 5 MG/ML Topical Lotion
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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".