NDC 61924-106 Gelrite
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What is NDC 61924-106?
What are the uses for Gelrite?
Which are Gelrite UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Gelrite 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)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O)
- PROPYLENE GLYCOL 1,2-DISTEARATE (UNII: T65PN3O37H)
- BUTANOL (MIXED ISOMERS) (UNII: WB09NY83YA)
- 2,4,5-T-TROLAMINE (UNII: 9007L1DAXM)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SODIUM ISOSTEAROYL LACTYLATE (UNII: 8730J0D3EV)
What is the NDC to RxNorm Crosswalk for Gelrite?
- RxCUI: 902574 - ethanol 65 % Topical Gel
- RxCUI: 902574 - ethanol 0.65 ML/ML Topical Gel
- RxCUI: 902574 - ethyl alcohol 65 % 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".