NDC 59779-588 Vagicaine Maximum Strength Anti-itch Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59779-588?
What are the uses for Vagicaine Maximum Strength Anti-itch Cream?
Which are Vagicaine Maximum Strength Anti-itch Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- RESORCINOL (UNII: YUL4LO94HK)
- RESORCINOL (UNII: YUL4LO94HK) (Active Moiety)
Which are Vagicaine Maximum Strength Anti-itch Cream 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-40 HYDROGENATED LANOLIN (UNII: 959P5CXE48)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- TROLAMINE (UNII: 9O3K93S3TK)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%) (UNII: L605B5892V)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- MINERAL OIL (UNII: T5L8T28FGP)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Vagicaine Maximum Strength Anti-itch Cream?
- RxCUI: 637518 - benzocaine 20 % / resorcinol 3 % Vaginal Cream
- RxCUI: 637518 - benzocaine 200 MG/ML / resorcinol 30 MG/ML Vaginal 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".