NDC 76982-3864 Linstol Refreshing And Cleansing Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76982 - Linstol Usa, Llc
- 76982-3864 - Linstol Refreshing And Cleansing Hand Sanitizer
Product Packages
NDC Code 76982-3864-0
Package Description: 2 mL in 1 PACKET
NDC Code 76982-3864-1
Package Description: 15 mL in 1 TUBE
NDC Code 76982-3864-2
Package Description: 30 mL in 1 BOTTLE, PLASTIC
NDC Code 76982-3864-3
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 76982-3864-4
Package Description: 118 mL in 1 BOTTLE, PLASTIC
NDC Code 76982-3864-5
Package Description: 236 mL in 1 BOTTLE, PUMP
NDC Code 76982-3864-6
Package Description: 500 mL in 1 BOTTLE, PUMP
NDC Code 76982-3864-7
Package Description: 532 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 76982-3864?
What are the uses for Linstol Refreshing And Cleansing Hand Sanitizer?
Which are Linstol Refreshing And Cleansing Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Linstol Refreshing And Cleansing Hand Sanitizer 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)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
- GLYCERIN (UNII: PDC6A3C0OX)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Linstol Refreshing And Cleansing Hand Sanitizer?
- RxCUI: 1305100 - ethanol 75 % Topical Gel
- RxCUI: 1305100 - ethanol 0.75 ML/ML Topical Gel
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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".