NDC 63868-115 Awaken By Quality Choice Foaming Hand Wash Spring Showers
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63868 - Chain Drug Marketing Association Inc
- 63868-115 - Awaken By Quality Choice Foaming Hand Wash
Product Packages
NDC Code 63868-115-07
Package Description: 222 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 63868-115?
What are the uses for Awaken By Quality Choice Foaming Hand Wash Spring Showers?
Which are Awaken By Quality Choice Foaming Hand Wash Spring Showers UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Awaken By Quality Choice Foaming Hand Wash Spring Showers 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE SODIUM (UNII: MP1J8420LU)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
What is the NDC to RxNorm Crosswalk for Awaken By Quality Choice Foaming Hand Wash Spring Showers?
- 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
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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".