NDC 63148-842 Giant Eagle Coconut Water Foaming
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63148 - Apollo Health And Beauty Care
- 63148-842 - Giant Eagle Coconut Water Foaming
Product Packages
NDC Code 63148-842-07
Package Description: 222 mL in 1 BOTTLE, PLASTIC
NDC Code 63148-842-08
Package Description: 222 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 63148-842?
What are the uses for Giant Eagle Coconut Water Foaming?
Which are Giant Eagle Coconut Water Foaming UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Giant Eagle Coconut Water Foaming 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)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- GLYCERIN (UNII: PDC6A3C0OX)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- COCONUT (UNII: 3RT3536DHY)
- BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SULISOBENZONE (UNII: 1W6L629B4K)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Giant Eagle Coconut Water Foaming?
- RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap
* 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".