DR.NUELL MUGWORT SHAKING PACK- glycerin liquid

Dr.NUELL Mugwort Shaking Pack by

Drug Labeling and Warnings

Dr.NUELL Mugwort Shaking Pack by is a Otc medication manufactured, distributed, or labeled by Apharm Co., Ltd., APHARM Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

glycerin

PURPOSE

dual functionality for brightening and wrinkle improvement certified

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

1. put 1st and 2nd packs in the pouch and seal them and shake them for 10 seconds

2. sweep the contents down and tear them along the bottom cut line

3. apply mixture to the fact with a sqag-hola and gently remove it from the bottom to the top after 20~30 minutes

4. remove the pack and apply skin product

WARNINGS

1) if there is any abnormal symptom or side effect, such as red spot, swelling and itching when using cosmetlcs or after using due to direct sunlight, consult dermatologists
2) Do not use for wounded areas
3) Precautions for storage and handling
keep out of reach of children, store away from direct sunlight
4) avoid the eye area

INACTIVE INGREDIENT

water, butylene glycol, 1,2-hexanediol, citric acid, etc

DOSAGE & ADMINISTRATION

For external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.NUELL MUGWORT SHAKING PACK 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73430-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	5.021 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73430-0002-1	70 g in 1 PACKAGE; Type 0: Not a Combination Product	11/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part347	11/01/2019

Labeler - Apharm Co., Ltd. (689054266)

Registrant - Apharm Co., Ltd. (689054266)

Establishment
Name	Address	ID/FEI	Business Operations
APHARM Co., Ltd.		689054266	manufacture(73430-0002)