NDC 61566-117 Burn Relief Extra Strength Kool-down
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61566 - Kool-down Inc
- 61566-117 - Burn Relief Extra Strength
Product Packages
NDC Code 61566-117-04
Package Description: 113 g in 1 BOTTLE
Product Details
What is NDC 61566-117?
What are the uses for Burn Relief Extra Strength Kool-down?
Which are Burn Relief Extra Strength Kool-down UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Burn Relief Extra Strength Kool-down 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 (UNII: V5VD430YW9)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- CERESIN (UNII: Q1LS2UJO3A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ALLANTOIN (UNII: 344S277G0Z)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TROLAMINE (UNII: 9O3K93S3TK)
- EDETATE SODIUM (UNII: MP1J8420LU)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALMOND OIL (UNII: 66YXD4DKO9)
- CANOLA OIL (UNII: 331KBJ17RK)
What is the NDC to RxNorm Crosswalk for Burn Relief Extra Strength Kool-down?
- RxCUI: 2108915 - lidocaine 3.9 % Topical Cream
- RxCUI: 2108915 - lidocaine 39 MG/ML Topical Cream
- RxCUI: 2108920 - Kool-Down 3.9 % Topical Cream
- RxCUI: 2108920 - lidocaine 39 MG/ML Topical Cream [Kool-Down]
- RxCUI: 2108920 - Kool-Down 39 MG/ML Topical Cream
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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".