NDC 49681-002 Vitale Sensitive Scalp 12 In 1 Instant Relief Anti Dandruff Spray
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49681 - Jf Labs, Inc.
- 49681-002 - Vitale Sensitive Scalp 12 In 1 Instant Relief Anti Dandruff Spray
Product Packages
NDC Code 49681-002-05
Package Description: 237 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 49681-002?
Which are Vitale Sensitive Scalp 12 In 1 Instant Relief Anti Dandruff Spray 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 Vitale Sensitive Scalp 12 In 1 Instant Relief Anti Dandruff Spray 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)
- ALCOHOL (UNII: 3K9958V90M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- CAMPHOR (UNII: 5TJD82A1ET)
- MENTHOL (UNII: L7T10EIP3A)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- SULFUR (UNII: 70FD1KFU70)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- EQUISETUM ARVENSE EXTRACT (UNII: 1L0VKZ185E)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
What is the NDC to RxNorm Crosswalk for Vitale Sensitive Scalp 12 In 1 Instant Relief Anti Dandruff Spray?
- RxCUI: 1042821 - salicylic acid 1.8 % Topical Spray
- RxCUI: 1042821 - salicylic acid 18 MG/ML Topical Spray
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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".