NDC 76466-500 Well At Walgreens Anti-itch Maximum Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76466 - Sci International
- 76466-500 - Well At Walgreens Anti-itch
Product Packages
NDC Code 76466-500-04
Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Details
What is NDC 76466-500?
What are the uses for Well At Walgreens Anti-itch Maximum Strength?
Which are Well At Walgreens Anti-itch Maximum Strength 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 Well At Walgreens Anti-itch Maximum Strength 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- LANOLIN (UNII: 7EV65EAW6H)
- POTASSIUM METHYLPARABEN (UNII: M64U971IB0)
- MINERAL OIL (UNII: T5L8T28FGP)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- TROLAMINE (UNII: 9O3K93S3TK)
- VITAMIN A (UNII: 81G40H8B0T)
- VITAMIN D (UNII: 9VU1KI44GP)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
What is the NDC to RxNorm Crosswalk for Well At Walgreens Anti-itch Maximum Strength?
- RxCUI: 637518 - benzocaine 20 % / resorcinol 3 % Vaginal Cream
- RxCUI: 637518 - benzocaine 200 MG/ML / resorcinol 30 MG/ML Vaginal 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".