NDC 80152-302 Zernel Scalp Rejuver Essence
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80152 - Zinozen Co., Ltd.
- 80152-302 - Zernel Scalp Rejuver Essence
Product Packages
NDC Code 80152-302-01
Package Description: 200 mL in 1 BOTTLE
Product Details
What is NDC 80152-302?
What are the uses for Zernel Scalp Rejuver Essence?
Which are Zernel Scalp Rejuver Essence UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Zernel Scalp Rejuver Essence 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:
- ALANINE (UNII: OF5P57N2ZX)
- ISOLEUCINE (UNII: 04Y7590D77)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- AMARANTHUS HYPOCHONDRIACUS SEED (UNII: TWW80P29UN)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- GLYCINE (UNII: TE7660XO1C)
- PROLINE (UNII: 9DLQ4CIU6V)
- HISTIDINE (UNII: 4QD397987E)
- CYSTINE (UNII: 48TCX9A1VT)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- WATER (UNII: 059QF0KO0R)
- PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- OCTYLDODECETH-25 (UNII: F8934HEL3M)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ALLANTOIN (UNII: 344S277G0Z)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- BETAINE (UNII: 3SCV180C9W)
- CHENOPODIUM QUINOA SEED (UNII: OO4K72NZ2X)
- GLUTAMIC ACID (UNII: 3KX376GY7L)
- LYSINE (UNII: K3Z4F929H6)
- LEUCINE (UNII: GMW67QNF9C)
- ARGININE (UNII: 94ZLA3W45F)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- LAVANDIN OIL (UNII: 9RES347CKG)
* 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".