FAMILY CARE MUSCLE AND JOINT VANISHING SCENT- menthol gel

FAMILY CARE MUSCLE AND JOINT VANISHING SCENT by

Drug Labeling and Warnings

FAMILY CARE MUSCLE AND JOINT VANISHING SCENT by is a Otc medication manufactured, distributed, or labeled by UNITED EXCHANGE CORP.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                                                              Purpose

Menthol 2.5%..................................................................................External Analgesic

PURPOSE

Uses

• For the temporary relief of minor aches and pains of muscles and joints associated with simple backaches, arthritis and sprains
  

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use with a Heating Pad, do not bandage tightly, do not swallow

KEEP OUT OF REACH OF CHILDREN

Keep Away from Children to Avoid Accidental Poisoning

ASK DOCTOR

If swallowed, induce vomiting and call a physician.  Keep away from eyes, mucous membranes, broken or irritated skin.  If skin redness or irritation develops, pain lasts more than 10 days. or with arthritis-like conditions in

children under 12, don not use and ask a doctor.

INDICATIONS & USAGE

Directions

• Apply generously and gently message until gel disappears
• Repeat 3 to 4 times daily
• Relief lasts for hours

For best results, squeeze tube from the bottom and flatten as you use products.

STORAGE AND HANDLING

Other information

• Store between 15 oC-30 oC (59 oF-86 oF)
• Lot No. and Exp. Date: see box or crimp of tube
  

INACTIVE INGREDIENT

Inactive ingredients

Carbomer 940, Potassium sorbate, Polysorbate 60, Trolamine, Isopropyl alcohol, Camphor, Methylparaben, Purified Water

DOSAGE & ADMINISTRATION

Distributed by:

UNITED EXCHANGE CORP.

17211 Valley View Ave.

Cerritos, CA 90703 USA

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FAMILY CARE MUSCLE AND JOINT VANISHING SCENT 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-514
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	2.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
POLYSORBATE 60 (UNII: CAL22UVI4M)
TROLAMINE (UNII: 9O3K93S3TK)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
METHYLPARABEN (UNII: A2I8C7HI9T)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-514-57	1 in 1 CARTON	11/24/2014
1		57 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	11/24/2014

Labeler - UNITED EXCHANGE CORP. (840130579)