Skip to main content

AAPE Hair Ampoule

Medically reviewed by Drugs.com. Last updated on Aug 16, 2021.

Dosage form: liquid
Ingredients: Panthenol 0.03g in 6mL
Labeler: PROSTEMICS Co., Ltd.
NDC Code: 62041-260

ACTIVE INGREDIENT

Active ingredients: Panthenol 0.5% 

INACTIVE INGREDIENT

Inactive ingredients:
Water, Alcohol, Propylene Glycol, Glycerin, Lactic Acid, Hydroxyacetophenone, Propanediol, Polyquaternium-7, Niacinamide, Polysorbate 20, Butylene Glycol, Caprylhydroxamic Acid, Disodium EDTA, Glycyrrhiza Glabra (Licorice) Root Extract, Camellia Sinensis Leaf Extract, Panax Ginseng Root Extract, Sophora, Angustifolia Root Extract, Angelica Gigas Root Extract, Cnidium Officinale Root Extract, Glycine Max (Soybean) Seed Extract, Polygonum Multiflorum Root Extract, 1,2-Hexanediol, Sodium Benzoate

PURPOSE

Purpose: Hair elasticity

WARNINGS

Warnings:
For external use only
1. Discontinue use if signs of irritation or rashes appear. If symptoms get worse, consult with a dermatologist. 1) In case of swelling, itching, or other side effects while or after using this product
2. Do not apply to open wounds.
3. Avoid contact with eyes.
Storage and handling
4. Keep in the refrigerator at 2-6°C.
5. Keep out of reach of children.
6. Avoid direct sunlight.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Uses

Uses:

Improves effects of hair elasticity.

Directions

Directions:

Gently mix with AAPE powder to dissolve the mixture.
Take proper amount and gently apply onto the scalp.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AAPE HAIR AMPOULE 
panthenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62041-260
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Panthenol (PANTHENOL) Panthenol0.03 g  in 6 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Alcohol 
Packaging
#Item CodePackage Description
1NDC:62041-260-016 mL in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/01/2019
Labeler - PROSTEMICS Co., Ltd. (689605919)
Registrant - PROSTEMICS Co., Ltd. (689605919)
Establishment
NameAddressID/FEIOperations
Prostemics Co., Ltd. Factory695687674manufacture(62041-260)

 
PROSTEMICS Co., Ltd.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.