NDC 11673-815 Up And Up Moisturizing Body Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11673 - Target Corporation
- 11673-815 - Up And Up
Product Packages
NDC Code 11673-815-21
Package Description: 621 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 11673-815?
What are the uses for Up And Up Moisturizing Body Wash?
Which are Up And Up Moisturizing Body Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Up And Up Moisturizing Body Wash 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)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- HYDROXYETHYL CELLULOSE (5000 CPS AT 1%) (UNII: X70SE62ZAR)
- GLYCERIN (UNII: PDC6A3C0OX)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POLOXAMER 124 (UNII: 1S66E28KXA)
- EDETATE SODIUM (UNII: MP1J8420LU)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- 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 Up And Up Moisturizing Body Wash?
- 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".