NDC 79512-009 Houdini Jr. Hand Sanitizer Peppermint Power
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79512 - Fantasma Toys
- 79512-009 - Houdini Jr. Hand Sanitizer Peppermint Power
Product Packages
NDC Code 79512-009-01
Package Description: 118 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 79512-009?
What are the uses for Houdini Jr. Hand Sanitizer Peppermint Power?
Which are Houdini Jr. Hand Sanitizer Peppermint Power UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Houdini Jr. Hand Sanitizer Peppermint Power 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:
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- 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 Jr. Hand Sanitizer Peppermint Power?
- 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".