NDC 81601-003 Handy Pocket Sanitizer Mist
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81601 - Cellicon Lab Inc.
- 81601-003 - Handy Pocket Sanitizer Mist
Product Packages
NDC Code 81601-003-01
Package Description: 20 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 81601-003?
What are the uses for Handy Pocket Sanitizer Mist?
Which are Handy Pocket Sanitizer Mist UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Handy Pocket Sanitizer Mist 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- OCTYLDODECETH-16 (UNII: RJV574G0DE)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- REYNOUTRIA JAPONICA ROOT (UNII: 7TRV45YZF7)
- PURSLANE (UNII: M6S840WXG5)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- CHAMOMILE (UNII: FGL3685T2X)
- ROSEMARY (UNII: IJ67X351P9)
What is the NDC to RxNorm Crosswalk for Handy Pocket Sanitizer Mist?
- RxCUI: 2535232 - ethanol 70.3 % Topical Spray
- RxCUI: 2535232 - ethanol 0.703 ML/ML Topical Spray
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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".