Label: THE QUEEN ROSE- witch hazel liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 55885-010-01 - Packager: LaLa Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 20, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
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
-
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
- INDICATIONS AND USAGE
- DOSAGE AND ADMINISTRATION
- PACKAGE LABEL. PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
THE QUEEN ROSE
witch hazel liquidProduct 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)