NDC 70993-0004 Atono2 Oxygen Bubble Foam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70993 - Laorganic Co., Ltd.
- 70993-0004 - Atono2 Oxygen Bubble Foam
Product Packages
NDC Code 70993-0004-1
Package Description: 150 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 70993-0004?
What are the uses for Atono2 Oxygen Bubble Foam?
Which are Atono2 Oxygen Bubble Foam UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Atono2 Oxygen Bubble Foam 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:
- BETAINE (UNII: 3SCV180C9W)
- WATER (UNII: 059QF0KO0R)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)
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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".