LIP AND HAND WILD ROSE- niacinamide, adenosine cream

Lip And Hand Wild Rose by

Drug Labeling and Warnings

Lip And Hand Wild Rose by is a Otc medication manufactured, distributed, or labeled by TOV Co., ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Niacinamide, Adenosine

INACTIVE INGREDIENT

Glycerin, Butylene Glycol, Etc.

PURPOSE

Hand Cream, Whitening, Anti Wrinkle

INDICATIONS & USAGE

1. Hand Cream : After Washing hands, Gently rub and massage hands with the hand cream.
2. Lip Balm : Apply the lip balm on lips for moisturizing.

DOSAGE & ADMINISTRATION

for external use only

WARNINGS

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIP AND HAND WILD ROSE 
niacinamide, adenosine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71077-0006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g  in 100 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.04 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71077-0006-1	30 mL in 1 TUBE; Type 0: Not a Combination Product	11/08/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/08/2016

Labeler - TOV Co., ltd (689851609)

Registrant - TOV Co., ltd (689851609)

Establishment
Name	Address	ID/FEI	Business Operations
TOV Co., ltd		689851609	manufacture(71077-0006)