NDC 69709-104 Notamo Hair Tonic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69709 - Hello International
- 69709-104 - Notamo Hair Tonic
Product Packages
NDC Code 69709-104-02
Package Description: 1 BOTTLE in 1 CARTON / 120 mL in 1 BOTTLE (69709-104-01)
Product Details
What is NDC 69709-104?
Which are Notamo Hair Tonic UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (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)
- PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- CORNUS OFFICINALIS FRUIT (UNII: 23NL8NQ187)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TARTARIC ACID (UNII: W4888I119H)
What is the NDC to RxNorm Crosswalk for Notamo Hair Tonic?
- RxCUI: 1741559 - salicylic acid 0.5 % / niacin amide 0.3 % Topical Spray
- RxCUI: 1741559 - niacinamide 3 MG/ML / salicylic acid 5 MG/ML Topical Spray
- RxCUI: 1741559 - niacinamide 0.3 % / salicylic acid 0.5 % Topical Spray
* 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".