NDC 70610-102 Greenfish, Body-s
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70610 - Kotuku Inc.
- 70610-102 - Greenfish, Body-s
Product Packages
NDC Code 70610-102-01
Package Description: 80 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 70610-102?
Which are Greenfish, Body-s UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
Which are Greenfish, Body-s 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CALCIUM HYDROXIDE (UNII: PF5DZW74VN)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- WATER (UNII: 059QF0KO0R)
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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".