NDC 21130-114 Signature Care Antibacterial Foaming Hand Pear Scent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21130 - Safeway Inc
- 21130-114 - Signature Care Antibacterial Foaming Hand Pear Scent
Product Packages
NDC Code 21130-114-07
Package Description: 222 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 21130-114?
What are the uses for Signature Care Antibacterial Foaming Hand Pear Scent?
Which are Signature Care Antibacterial Foaming Hand Pear Scent UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Signature Care Antibacterial Foaming Hand Pear Scent 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)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SODIUM PHOSPHATE, DIBASIC ANHYDROUS (UNII: 22ADO53M6F)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Signature Care Antibacterial Foaming Hand Pear Scent?
- RxCUI: 1053855 - triclosan 0.46 % Medicated Liquid Soap
- RxCUI: 1053855 - triclosan 4.6 MG/ML Medicated Liquid Soap
- RxCUI: 1053855 - triclosan 0.46 % Foaming Medicated Hand 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".