NDC 69709-102 Notamo Hair Tonic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69709 - Hello International
- 69709-102 - Notamo Hair Tonic
Product Packages
NDC Code 69709-102-02
Package Description: 1 BOTTLE, SPRAY in 1 PACKAGE / 120 mL in 1 BOTTLE, SPRAY (69709-102-01)
Product Details
What is NDC 69709-102?
Which are Notamo Hair Tonic UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- DEXPANTHENOL (UNII: 1O6C93RI7Z) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Notamo Hair Tonic 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)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- DODECYLAMINE (UNII: YWY9OD6A2K)
- PIROCTONE OLAMINE (UNII: A4V5C6R9FB)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
What is the NDC to RxNorm Crosswalk for Notamo Hair Tonic?
- RxCUI: 1648152 - salicylic acid 0.25 % / dexpanthenol 0.2 % Topical Solution
- RxCUI: 1648152 - dexpanthenol 2 MG/ML / salicylic acid 2.5 MG/ML Topical Solution
- RxCUI: 1648152 - dexpanthenol 0.2 % / salicylic acid 0.25 % Topical Solution
* 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".