NDC 79512-008 Houdini Hand Sanitizer Ocean Mist
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79512 - Fantasma Toys
- 79512-008 - Houdini Hand Sanitizer Ocean Mist
Product Packages
NDC Code 79512-008-01
Package Description: 236.5 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 79512-008?
What are the uses for Houdini Hand Sanitizer Ocean Mist?
Which are Houdini Hand Sanitizer Ocean Mist UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Houdini Hand Sanitizer Ocean 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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- WATER (UNII: 059QF0KO0R)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Houdini Hand Sanitizer Ocean Mist?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % 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".