NDC 49681-001 Vitale Sensitive Scalp Daily Scalp Healer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49681 - New Life Products, Inc.
- 49681-001 - Vitale Sensitive Scalp Daily Scalp Healer
Product Characteristics
Product Packages
NDC Code 49681-001-01
Package Description: 114 g in 1 JAR
Product Details
What is NDC 49681-001?
What are the uses for Vitale Sensitive Scalp Daily Scalp Healer?
Which are Vitale Sensitive Scalp Daily Scalp Healer UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5) (Active Moiety)
Which are Vitale Sensitive Scalp Daily Scalp Healer 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- 1,3-DIMETHYLOL-5,5-DIMETHYL-HYDANTOIN (UNII: BYR0546TOW)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WAX, YELLOW (UNII: 2ZA36H0S2V)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- MENTHOL (UNII: L7T10EIP3A)
- EQUISETUM ARVENSE EXTRACT (UNII: 1L0VKZ185E)
- STEARALKONIUM CHLORIDE (UNII: 0OUO26BB88)
- CAMPHOR (UNII: 5TJD82A1ET)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BIOTIN (UNII: 6SO6U10H04)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MINERAL OIL (UNII: T5L8T28FGP)
What is the NDC to RxNorm Crosswalk for Vitale Sensitive Scalp Daily Scalp Healer?
- RxCUI: 259549 - zinc pyrithione 0.25 % Topical Cream
- RxCUI: 259549 - zinc pyrithione 2.5 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".