NDC 59779-272 Cvs White Tea
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy
- 59779-272 - Cvs
Product Packages
NDC Code 59779-272-10
Package Description: 295 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 59779-272?
What are the uses for Cvs White Tea?
Which are Cvs White Tea UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Cvs White Tea 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- GLYCERIN (UNII: PDC6A3C0OX)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- POLOXAMER 124 (UNII: 1S66E28KXA)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
What is the NDC to RxNorm Crosswalk for Cvs White Tea?
- RxCUI: 1049254 - benzalkonium chloride 0.13 % Topical Solution
- RxCUI: 1049254 - benzalkonium chloride 1.3 MG/ML Topical Solution
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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".