NDC 82246-000 Stranded Hand Sanitizing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82246 - Annalo Industries, Llc
- 82246-000 - Stranded Hand Sanitizing
Product Packages
NDC Code 82246-000-01
Package Description: 60 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 82246-000?
What are the uses for Stranded Hand Sanitizing?
Which are Stranded Hand Sanitizing UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Stranded Hand Sanitizing 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)
- C13-15 ALKANE (UNII: 114P5I43UJ)
- SHEA BUTTER (UNII: K49155WL9Y)
- GLYCERIN (UNII: PDC6A3C0OX)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- CANDELILLA WAX (UNII: WL0328HX19)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WEST INDIAN LEMONGRASS OIL (UNII: 5BIA40E9ED)
- CLARY SAGE OIL (UNII: 87L0D4U3M0)
- CLOVE OIL (UNII: 578389D6D0)
- CITRUS SINENSIS FRUIT OIL (UNII: WV48LBL15Q)
- ROSEMARY OIL (UNII: 8LGU7VM393)
What is the NDC to RxNorm Crosswalk for Stranded Hand Sanitizing?
- RxCUI: 1809903 - ethanol 70 % Topical Lotion
- RxCUI: 1809903 - ethanol 0.7 ML/ML Topical Lotion
* Please review the disclaimer below.
[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".