AAPE NUTRIENT FACIAL TONER- niacinamide liquid

AAPE Nutrient Facial Toner by

Drug Labeling and Warnings

AAPE Nutrient Facial Toner by is a Otc medication manufactured, distributed, or labeled by PROSTEMICS Co., Ltd., Prostemics Co., Ltd. Factory. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Niacinamide 2.00%

INACTIVE INGREDIENT

Inactive ingredients:
Water, Butylene Glycol, PEG/PPG-17/6 Copolymer, Trehalose, Human Adipocyte Conditioned Media Extract, 1,2-Hexanediol, Caprylyl Glycol, Bis-PEG-18 Methyl Ether Dimethyl Silane, Ethylhexylglycerin, Salix Alba (Willow) Bark Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tromethamine, Glycerin, Cellulose Gum, Panthenol, PEG-60 Hydrogenated Castor Oil, Hamamelis Virginiana (Witch Hazel) Leaf Water, Disodium EDTA, Glyceryl Citrate/Lactate/Linoleate/Oleate, Sodium Hyaluronate, Olea Europaea (Olive) Fruit Oil, Polysorbate 60, Lilium Candidum, Flower Extract, Leontopodium Alpinum Flower/Leaf Extract, Convallaria Majalis Bulb/Root Extract, Magnolia Liliflora Flower Extract, Paeonia Lactiflora Extract, Palmitoyl Tripeptide-5, Fragrance

PURPOSE

Purpose: Skin Brightening

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. Replace the cap after use
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:

Helps brighten skin tone.

Directions

Directions:

Take proper amount and gently apply onto the face.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AAPE NUTRIENT FACIAL TONER 
niacinamide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62041-200
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	Niacinamide	2.60 g  in 130 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62041-200-02	1 in 1 CARTON	08/01/2019
1	NDC: 62041-200-01	130 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/01/2019

Labeler - PROSTEMICS Co., Ltd. (689605919)

Registrant - PROSTEMICS Co., Ltd. (689605919)

Establishment
Name	Address	ID/FEI	Business Operations
Prostemics Co., Ltd. Factory		695687674	manufacture(62041-200)