NDC 76767-020 G Sol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76767 - Egtech Co., Ltd.
- 76767-020 - G Sol
Product Packages
NDC Code 76767-020-01
Package Description: 30 mL in 1 BOTTLE, SPRAY
NDC Code 76767-020-02
Package Description: 60 mL in 1 BOTTLE, SPRAY
NDC Code 76767-020-03
Package Description: 450 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 76767-020?
What are the uses for G Sol?
Which are G Sol UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
Which are G Sol 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)
- SORBITAN (UNII: 6O92ICV9RU)
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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".