NDC 36800-718 Bite And Sting Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 36800 - Top Care
- 36800-718 - Bite And Sting Relief
Product Packages
NDC Code 36800-718-02
Package Description: 1 TUBE in 1 CARTON / 50 g in 1 TUBE
Product Details
What is NDC 36800-718?
What are the uses for Bite And Sting Relief?
Which are Bite And Sting Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Bite And Sting Relief 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)
- PEG-2 STEARATE (UNII: 94YQ11Y95F)
- ALCOHOL (UNII: 3K9958V90M)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- HYDROCORTISONE (UNII: WI4X0X7BPJ)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CHAMOMILE (UNII: FGL3685T2X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- MENTHOL (UNII: L7T10EIP3A)
- PEPPERMINT (UNII: V95R5KMY2B)
- CLOVE OIL (UNII: 578389D6D0)
- PAPAIN (UNII: A236A06Y32)
What is the NDC to RxNorm Crosswalk for Bite And Sting Relief?
- RxCUI: 198494 - benzocaine 5 % Topical Cream
- RxCUI: 198494 - benzocaine 50 MG/ML Topical Cream
* 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".