NDC 76348-575 Ak47 Menthol Warming
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76348 - Renu Laboratories, Inc.
- 76348-575 - Ak47 Menthol Warming
Product Packages
NDC Code 76348-575-10
Package Description: 10 PACKET in 1 BOX / 4 g in 1 PACKET (76348-575-04)
Product Details
What is NDC 76348-575?
What are the uses for Ak47 Menthol Warming?
Which are Ak47 Menthol Warming UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Ak47 Menthol Warming 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:
- OLIVE OIL (UNII: 6UYK2W1W1E)
- CORN OIL (UNII: 8470G57WFM)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- TABASCO PEPPER (UNII: J1M3NA843L)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CARYOPHYLLENE (UNII: BHW853AU9H)
- PINENE (UNII: 996299PUKB)
- TERPINEOL (UNII: R53Q4ZWC99)
- COCONUT OIL (UNII: Q9L0O73W7L)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MYRCENE (UNII: 3M39CZS25B)
- WATER (UNII: 059QF0KO0R)
- WHITE WAX (UNII: 7G1J5DA97F)
- WITCH HAZEL (UNII: 101I4J0U34)
- MANGIFERA INDICA SEED BUTTER (UNII: 4OXD9M35X2)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- SHEA BUTTER (UNII: K49155WL9Y)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LAURETH-7 (UNII: Z95S6G8201)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- STEARIC ACID (UNII: 4ELV7Z65AP)
* 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".