THE QUEEN ROSE- witch hazel liquid

THE QUEEN ROSE by

Drug Labeling and Warnings

THE QUEEN ROSE by is a Otc medication manufactured, distributed, or labeled by LaLa Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient: Witch Hazel 0.1%

INACTIVE INGREDIENT

Inactive ingredients:
ANISE OIL, BERGAMOT OIL, CHAMOMILLE ROMAN OIL, GERANIUM OIL, LAVENDER OIL, LEMON OIL, ORANGE OIL, OLIVE OIL, ROSE BULGARIA OIL, YLANG YLANG OIL, SUN FLOWER OIL, LEONURUS SIBIRICUS EXTRACT, ANGELICA GIGAS ROOT EXTRACT, ARTEMISIA PRINCEPS LEAF EXTRACT, CHRYSANTHEMUM ZAWADSKII EXTRACT

PURPOSE

Purpose: Skin Protectant, Fragrance

WARNINGS

Warnings:
In case of having following symptoms after using this, you're advised to stop using it immediately.
If you keep using it, the symptoms will get worse and need to consult a dermatologist.
1) In case of having problems such as red rash, swollenness, itching, stimulation during usage.
2) In case of having the same symptoms above on the part you put this product on by direct sunlight.
You are banned to use it on the part where you have a scar, eczema, or dermatitis.
In case of getting it into your eyes, you have to wash it immediately.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:
Keep out of reach of babies and children.

INDICATIONS AND USAGE

Indication and usage:
Tighten the lid after using it.
Keep it out of infants or children's reach.
Don't keep it in the place where the temperature is extremely hot or low and exposed to the direct sunlight.

DOSAGE AND ADMINISTRATION

Dosage and administration:
Tighten the lid after using it.
Keep it out of infants or children's reach.
Don't keep it in the place where the temperature is extremely hot or low and exposed to the direct sunlight.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

THE QUEEN ROSE 
witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55885-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	0.005 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
ANISE OIL (UNII: 6Y89129C8H)
BERGAMOT OIL (UNII: 39W1PKE3JI)
GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55885-010-01	5 mL in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	12/01/2012

Labeler - LaLa Co., Ltd. (688380004)

Registrant - LaLa Co., Ltd. (688380004)

Establishment
Name	Address	ID/FEI	Business Operations
LaLa Co., Ltd.		688380004	manufacture(55885-010)