NDC 57367-007 Nick Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57367 - 220 Laboratories Inc
- 57367-007 - Nick Relief
Product Packages
NDC Code 57367-007-20
Package Description: 1 APPLICATOR in 1 BLISTER PACK / 7 mL in 1 APPLICATOR (57367-007-07)
Product Details
What is NDC 57367-007?
What are the uses for Nick Relief?
Which are Nick Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM SULFATE (UNII: 34S289N54E)
- ALUMINUM CATION (UNII: 3XHB1D032B) (Active Moiety)
Which are Nick 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)
- WITCH HAZEL (UNII: 101I4J0U34)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIAZOLIDINYLUREA (UNII: H5RIZ3MPW4)
- PANTHENOL (UNII: WV9CM0O67Z)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- MELISSA OFFICINALIS (UNII: YF70189L0N)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GERANIUM EXTRACT (UNII: 6H429I0Y3L)
- QUERCUS ALBA (UNII: XR6BC2ZUAM)
- ROSA CANINA FRUIT (UNII: 3TNW8D08V3)
- SAGE (UNII: 065C5D077J)
- COMFREY (UNII: D05HXK6R3G)
- YARROW FLOWER (UNII: YQR8R0SQEA)
- EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
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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".