NDC 25225-019 Pomegranate Rose Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 25225 - Unique Holding Group Inc
- 25225-019 - Pomegranate Rose Hand Sanitizer
Product Packages
NDC Code 25225-019-01
Package Description: 28 g in 1 BOTTLE, PLASTIC
NDC Code 25225-019-02
Package Description: 59 g in 1 BOTTLE, PLASTIC
NDC Code 25225-019-03
Package Description: 222 g in 1 BOTTLE, PLASTIC
NDC Code 25225-019-04
Package Description: 237 g in 1 BOTTLE, PLASTIC
NDC Code 25225-019-05
Package Description: 500 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 25225-019?
What are the uses for Pomegranate Rose Hand Sanitizer?
Which are Pomegranate Rose Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Pomegranate Rose Hand Sanitizer 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- TROLAMINE (UNII: 9O3K93S3TK)
- POMEGRANATE (UNII: 56687D1Z4D)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Pomegranate Rose Hand Sanitizer?
- RxCUI: 581660 - ethanol 62 % Topical Gel
- RxCUI: 581660 - ethanol 0.62 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".