NDC 74657-015 Aloha Gel Hand Sanitizer Crazy Coconut
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 74657 - Double Body Biotech Limited
- 74657-015 - Aloha Gel Hand Sanitizer Crazy Coconut
Product Packages
NDC Code 74657-015-01
Package Description: 60 mL in 1 BOTTLE
Product Details
What is NDC 74657-015?
What are the uses for Aloha Gel Hand Sanitizer Crazy Coconut?
Which are Aloha Gel Hand Sanitizer Crazy Coconut UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Aloha Gel Hand Sanitizer Crazy Coconut 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:
- ETHYL BUTYRATE (UNII: UFD2LZ005D)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARBOMER 980 (UNII: 4Q93RCW27E)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- GERANIOL (UNII: L837108USY)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- RACEMENTHOL (UNII: YS08XHA860)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- COUMARIN (UNII: A4VZ22K1WT)
- .GAMMA.-NONALACTONE (UNII: I1XGH66S8P)
- P-ANISALDEHYDE (UNII: 9PA5V6656V)
- BENZYL BENZOATE (UNII: N863NB338G)
What is the NDC to RxNorm Crosswalk for Aloha Gel Hand Sanitizer Crazy Coconut?
- 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".