NDC 69224-2001 Ac All

  1. Labeler Index
  2. Gl Biotech
  3. NDC: 69224-2001 Ac All

NDC Product Code 69224-2001

NDC CODE: 69224-2001

Proprietary Name: Ac All 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 69224-2001-1

Package Description: 30 mL in 1 BOTTLE

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

NDC Product Information

Ac All with NDC 69224-2001 is a product labeled by Gl Biotech. The generic name of Ac All is . The product's dosage form is and is administered via form.

Labeler Name: Gl Biotech

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.
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Product Labeler Information

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

Labeler Name: Gl Biotech
Labeler Code: 69224
Start Marketing Date: 10-17-2014 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.

Ac All Product Label Images

Ac All 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

Blueberry ext, assai ext, indian gooseberry fruit ext, cranberry fruit ext, melon ext, rhus tree bark ext, lactobacillus, colloidal silver, lavender oil, etc

Otc - Purpose

Skin protectionexcellent antimicrobialsafe for human body

Otc - Keep Out Of Reach Of Children

Keep out or reach of the children

Indications & Usage

1. Put 1-2 drops of AC ALL spot care ampule liquid on cotton bud or a vessel.2. Place watery cotton bud on the skin and gently push for 5 minutes until absorbed.3. Repeat 1 and 2 for 2-3 times, and 2 times a day.4. When suppuration has occurred as a secondary infection, remove it before use.5. Put a cotton swab dipped into the ampule lightly on the reddened spot for 5 seconds.6. Use lotions after the liquid is fully absorbed on skin.7. Trouble spots will disappear in 2-3 days, and generally skin will be improved in 1-2months.8. Use repetitively on troubled skin (Red or black marks) until the skin condition becamebetter.(Do not reuse the cotton bud due to the risk of bacterial infection.)

Warnings

- avoid direct sun exposure, keep it refrigerated or in cooler places- do not eat

Dosage & Administration

For exernal use only

* Please review the disclaimer below.