NDC 80984-002 The Germ Assassin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 80984-002-01
Package Description: 60 mL in 1 BOTTLE
NDC Code 80984-002-02
Package Description: 100 mL in 1 BOTTLE
NDC Code 80984-002-03
Package Description: 237 mL in 1 BOTTLE
NDC Code 80984-002-04
Package Description: 500 mL in 1 BOTTLE
NDC Code 80984-002-05
Package Description: 473 mL in 1 BOTTLE
NDC Code 80984-002-06
Package Description: 945 mL in 1 BOTTLE
NDC Code 80984-002-07
Package Description: 3800 mL in 1 BOTTLE
NDC Code 80984-002-09
Package Description: 4000 mL in 1 BOTTLE
Product Details
What is NDC 80984-002?
What are the uses for The Germ Assassin?
Which are The Germ Assassin UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are The Germ Assassin 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- TROLAMINE (UNII: 9O3K93S3TK)
- DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
- WATER (UNII: 059QF0KO0R)
- MENTHA SPICATA OIL (UNII: C3M81465G5)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- TEA TREE OIL (UNII: VIF565UC2G)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- COCONUT OIL (UNII: Q9L0O73W7L)
- ORANGE OIL (UNII: AKN3KSD11B)
- ALOE (UNII: V5VD430YW9)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)
What is the NDC to RxNorm Crosswalk for The Germ Assassin?
- RxCUI: 1047755 - ethanol 75 % Topical Solution
- RxCUI: 1047755 - ethanol 0.75 ML/ML Topical Solution
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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".