NDC 71884-030 Triple Shield Sanitizing Hand Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71884 - Enviro Specialty Chemicals Inc
- 71884-030 - Triple Shield Sanitizing Hand Wipes
Product Packages
NDC Code 71884-030-20
Package Description: 20 PATCH in 1 PACKET / 5.25 mL in 1 PATCH
Product Details
What is NDC 71884-030?
What are the uses for Triple Shield Sanitizing Hand Wipes?
Which are Triple Shield Sanitizing Hand Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Triple Shield Sanitizing Hand Wipes 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
- LAURETH-4 (UNII: 6HQ855798J)
- POLIHEXANIDE (UNII: 322U039GMF)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)
What is the NDC to RxNorm Crosswalk for Triple Shield Sanitizing Hand Wipes?
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Swab
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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".