NDC 70993-0004 Atono2 Oxygen Bubble Foam

NDC Product Code 70993-0004

NDC CODE: 70993-0004

Proprietary Name: Atono2 Oxygen Bubble Foam What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

  • 70993 - Laorganic Co., Ltd.

NDC 70993-0004-1

Package Description: 150 mL in 1 BOTTLE, PUMP

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Atono2 Oxygen Bubble Foam with NDC 70993-0004 is a product labeled by Laorganic Co., Ltd.. The product's dosage form is and is administered via form.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • BETAINE (UNII: 3SCV180C9W)
  • WATER (UNII: 059QF0KO0R)
  • DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
  • DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Laorganic Co., Ltd.
Labeler Code: 70993
Start Marketing Date: 11-01-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Atono2 Oxygen Bubble Foam Product Label Images

Atono2 Oxygen Bubble Foam Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Glycerin

Inactive Ingredient

Disodium Cocoyl Glutamate, Decyl Glucoside, Potassium Cocoyl Glycinate, Disodium Cocoamphodiacetate, Betaine, Potassium Cocoate, Panthenol, etc.

Otc - Purpose

Skin Protectant

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Pump an appropriate amount and gently massage the wet facial skin with it. Then rinse with warm water.

Warnings

  • For external use onlyWhen using this product1. If any one of following symptoms occurs when using cosmetics, stop using it and consult a dermatologist.
  • A. red spot, swelling, itching, stimulus
  • B. symptoms mentioned above are caused by sunlight.
  • 2. Do not apply on skin where there is wound, eczema, or irritation.3. Storage and cautions for handling
  • A. Close stopper after using.
  • B. Keep out of reach of children.
  • C. Keep away from high or low temperature and direct sunlight.
  • 4. This is not a medicinal product. Made of 100% cosmetic ingredients, it is a sensitive-skin care product for all skin types.

Dosage & Administration

For external use only

* Please review the disclaimer below.