NDC 59779-436 Healing Cvs
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs
- 59779-436 - Healing
Product Packages
NDC Code 59779-436-04
Package Description: 113 g in 1 JAR
Product Details
What is NDC 59779-436?
What are the uses for Healing Cvs?
Which are Healing Cvs UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Healing Cvs 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- OAT (UNII: Z6J799EAJK)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CHAMOMILE (UNII: FGL3685T2X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CURDLAN (UNII: 6930DL209R)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBITOL (UNII: 506T60A25R)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- XANTHAN GUM (UNII: TTV12P4NEE)
- OLEIC ACID (UNII: 2UMI9U37CP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
What is the NDC to RxNorm Crosswalk for Healing Cvs?
- RxCUI: 1442087 - allantoin 0.5 % Topical Gel
- RxCUI: 1442087 - allantoin 0.005 MG/MG Topical Gel
* 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".