NDC 70540-030 Hyundae Meditech Bio Hair Solu Tion Erua Do

NDC Product Code 70540-030

NDC 70540-030-02

Package Description: 12 VIAL in 1 CARTON > 5 g in 1 VIAL (70540-030-01)

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

NDC Product Information

Hyundae Meditech Bio Hair Solu Tion Erua Do with NDC 70540-030 is product labeled by Innogene 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)

Product Labeler Information

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

Labeler Name: Innogene Co.,ltd
Labeler Code: 70540
Start Marketing Date: 08-20-2016 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.

Hyundae Meditech Bio Hair Solu Tion Erua Do Product Label Images

Hyundae Meditech Bio Hair Solu Tion Erua Do 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: Allantoin 0.95%

Inactive Ingredient

Inactive Ingredients: Water, Glycerin, Butylene Glycol, Methylparaben, Phenoxyethanol, Sorbitol, Glycogen, Copper Tripeptide-1, Mannitol, Pterocarpus Marsupium Bark Extract, Serenoa Serrulata Fruit Extract, Ammonium Glycyrrhizate, Disodium Succinate, Eriobotrya Japonica Leaf Extract, Glutamic Acid, Caffeine, Zinc Gluconate, Aesculus Hippocastanum (Horse Chestnut) Seed Extract


Purpose: Scalp Protectant


Warnings: 1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms): a) Red spots, swelling, itchiness, and other skin irritation b) If the symptoms above occur after the application area is exposed to direct sunlight. 2. Do not use on open wounds, eczema, and other skin irritations. 3. Storing and handling a) Close the lid after every use. b) Keep out of reach of infants and children. c) Do not store at extreme temperatures or in an area exposed to direct sunlight. 4. Wash away immediately when permeating into the eyes.

Keep Out Of Reach Of Children

Keep out of reach of infants and children.

Indications & Usage

Indications & usage: 1. Wash scalp tholoughly before product use. 2. Shake the product. 3. Take appropriate amount out of a container and rub on parts of scalp in trouble to absorb enough.

Dosage & Administration

Dosage & Administration: One time per week, 5cc for one use

* Please review the disclaimer below.