NDC 62839-2810 Epoch Ava Puhi Moni
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62839 - Nse Products, Inc.
- 62839-2810 - Epoch
Product Packages
NDC Code 62839-2810-1
Package Description: 250 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 62839-2810?
What are the uses for Epoch Ava Puhi Moni?
Which are Epoch Ava Puhi Moni 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 Epoch Ava Puhi Moni 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)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CLEMATIS VITALBA LEAF (UNII: 526T95850X)
- MAHONIA AQUIFOLIUM ROOT (UNII: 746TB9VNDP)
- SAGE (UNII: 065C5D077J)
- URTICA DIOICA (UNII: 710FLW4U46)
- PANTHENOL (UNII: WV9CM0O67Z)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SODIUM COPPER CHLOROPHYLLIN (UNII: 1D276TYV9O)
What is the NDC to RxNorm Crosswalk for Epoch Ava Puhi Moni?
- RxCUI: 1242148 - epoch Anti-Dandruff 1 % Medicated Shampoo
- RxCUI: 1242148 - zinc pyrithione 10 MG/ML Medicated Shampoo [Epoch Anti-Dandruff]
- RxCUI: 1242148 - Epoch Anti-Dandruff 10 MG/ML Medicated Shampoo
- RxCUI: 1242148 - Epoch Ava Puhi Moni 1 % Anti-Dandruff Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
* 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".