NDC 90107-1560 After Bite Outdoor
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 90107 - Adventure Ready Brands
- 90107-1560 - After Bite Outdoor
Product Packages
NDC Code 90107-1560-0
Package Description: 20 g in 1 TUBE
NDC Code 90107-1560-1
Package Description: 1 TUBE in 1 BOX / 20 g in 1 TUBE
Product Details
What is NDC 90107-1560?
What are the uses for After Bite Outdoor?
Which are After Bite Outdoor UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
Which are After Bite Outdoor 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ALCOHOL (UNII: 3K9958V90M)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- TEA TREE OIL (UNII: VIF565UC2G)
- METHYLCELLULOSE (100 CPS) (UNII: 4GFU244C4J)
- OATMEAL (UNII: 8PI54V663Y)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for After Bite Outdoor?
- RxCUI: 1049880 - diphenhydrAMINE HCl 2 % Topical Gel
- RxCUI: 1049880 - diphenhydramine hydrochloride 0.02 MG/MG Topical Gel
- RxCUI: 1049880 - diphenhydramine hydrochloride 2 % Topical Gel
* Please review the disclaimer below.
[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".