NDC 70749-010 Znsp Ampoule

NDC Product Code 70749-010

NDC CODE: 70749-010

Proprietary Name: Znsp Ampoule 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

  • 70749 - Z-ton Es Bio Co., Ltd.

NDC 70749-010-02

Package Description: 15 BOTTLE in 1 CARTON > 5 mL in 1 BOTTLE (70749-010-01)

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

NDC Product Information

Znsp Ampoule with NDC 70749-010 is a product labeled by Z-ton Es Bio 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.

  • WATER (UNII: 059QF0KO0R)
  • METHYLPROPANEDIOL (UNII: N8F53B3R4R)

Product Labeler Information

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

Labeler Name: Z-ton Es Bio Co., Ltd.
Labeler Code: 70749
Start Marketing Date: 05-01-2016 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: 12-31-2018 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.

Znsp Ampoule Product Label Images

Znsp Ampoule 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

Active Ingredient

Active Ingredient: GLYCERIN 5.0%

Inactive Ingredient

Inactive Ingredients: WATER, ACETYL HEXAPEPTIDE-8, Methyl PROPANDIOL, ARBUTINE, CITRUSPARADISI(GRAPEFRUIT)FRUIT EXTRACT, SCUTELLARIA BAICALENSISROOT EXTRACT, PAEONIA SUFFRUTICOSAROOT EXTRACT, 1,2-HEXANDIOL, SODIUM HYALURONATE, CARBOMER, ADENOSINE, DISODIUM EDTA

Purpose

Purpose: Skin Protectant

Warnings

Warnings: 1. It is recommended to stop applying and consult a doctor immediately if you are suffering such conditions A) In case of rash, swell-up, itchiness B) If applied part is suffering conditions above on direct exposure to sunlight 2. Do not apply directly to wound or open cut 3. Cautions on storage A) Keep the cap sealed B) Away from children C) Do not leave it on high, low temperature or exposed on sunlight

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Indications & Usage

Indications & usage: 1. Carefully open the ampoule2-1. Without compressor: Apply an appropriate amount of the product on the clean face skin. Gently smooth over entire face to help the absorption of the product.2-2. With compressor: insert one ampoule into compressor and gently spray it all over the face.

Dosage & Administration

Dosage & Administration: Apply 2ml per each time; gently wrap your skin to help absorption

* Please review the disclaimer below.