YUN XIANG JING- menthol liniment

YUN XIANG JING by

Drug Labeling and Warnings

YUN XIANG JING by is a Otc medication manufactured, distributed, or labeled by GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients
Menthol 3%

PURPOSE

Purpose
External Analgesic

INDICATIONS & USAGE

Uses
For the temporary relief of minor aches and pains of muscles and joints due to:
simple backache
arthritis
strains
bruises
sprains

WARNINGS

Warnings
For external use only
Do not use
on wounds
on irritated or damaged skin

WHEN USING

When using this product
avoid contact with the eyes and mucous membranes
do not bandage tightly

STOP USE

Stop use and ask a doctor if
condition worsens
symptoms persist for more than 7 days
symptoms clear up and occur again within a few days
excessive irritation of the skin develops
when using for pain of arthritis:
if pain persists for more than 10 days
if redness is present
in conditions affecting children under 12 years of age

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions
Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
Children under 2 years of age: Do not use, consult a doctor.

STORAGE AND HANDLING

Other Information
keep tightly sealed
store in a cool, 8° to 15° C (46° to 59° F), dry place

INACTIVE INGREDIENT

Inactive Ingredients
Cinnamon (gui zhi) twig extract, hance pepper (san ju) rhizome extract, St. Thomas bean (guo gang long) stem extract, sparganium (san leng) rhizome extract, tinospora (jin guo lan) root extract, and water.

QUESTIONS

Questions or Comments? (888) 221-3496 M-F 9 am to 5 pm

PRINCIPAL DISPLAY PANEL

YUN XIANG JING

NDC: 59321-033-01

External Analgesic

1 Fl Oz (30 mL)

INGREDIENTS AND APPEARANCE

YUN XIANG JING 
menthol liniment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59321-033
Route of Administration	PERCUTANEOUS, TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CHINESE CINNAMON (UNII: WS4CQ062KM)
ENTADA PHASEOLOIDES WHOLE (UNII: 676S281WTB)
SPARGANIUM STOLONIFERUM ROOT (UNII: 66ZQ85S65H)
TINOSPORA CAPILLIPES ROOT (UNII: U65RN3L8Q5)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59321-033-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/08/2002

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/08/2002

Labeler - GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD (653862581)

Establishment
Name	Address	ID/FEI	Business Operations
GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD		653862581	manufacture(59321-033)