FAMILY CARE PAIN RELIEF- dl-camphor, l-menthol, methylsalicylate patch

Family Care Pain Relief by

Drug Labeling and Warnings

Family Care Pain Relief 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 Ingredients                                                            Purpose

DL-Camphor 1.2%....................................................Topical Analgesic

L-Menthol 5.7%........................................................Topical Analgesic

Methylsalicylate 6.3%................................................Topical Analgesic

PURPOSE

Uses

For temporary relief of minor aches and pains of muscles and joints associated with:

• arthritis
• simple backaches
• strains
• bruises
• sprains

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use

• on wounds or damaged skin
• if you are allergic to aspirin or salicylates
• with a heating pad
• with, or at the same time as, other external analgesic products

ASK DOCTOR

Ask a doctor before use, if you are allergic to any ingredients in this product

WHEN USING

When using this product

• do not use otherwise than directed
• avoid contact with the eyes, mucous membranes or rashes

STOP USE

Stop use and ask a doctore if

• rash, itching or excessive skin irritation develops
• conditions worsen
• symptoms persist for more than 7 days
• symptoms clear up and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children, if swallowed, get medical help or contact a Poision Control Center right away

INDICATIONS & USAGE

Directions

Aduts and children 12 years of age and over:

• clean and dry affected area
• remove patch from film
• apply to affected area no more than 3 to 4 times daily for 7 days
• remove patch from skin after at most 8 hours of application

Children under 12 years of age:

• consult a doctor

STORAGE AND HANDLING

Other Information

• avoid storing product in direct sunlight
• protect from excessive moisture

INACTIVE INGREDIENT

Inactive Ingredients

BHT, calcium carbonate, C4-6 oletin / styrene copolymer, glycerol abietate, isopropyl myristate, polybutene, polyisobutene, propylene carbonate, rubber latex, sorbitian stearate, ys resin, zinc oxide

DOSAGE & ADMINISTRATION

DISTRIBUTED BY:

UNITED EXCHANGE CORP.

17211 VALLEY VIEW AVE.

CERRITOS, CA 90703

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FAMILY CARE PAIN RELIEF 
dl-camphor, l-menthol, methylsalicylate patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-385
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	1.2 g  in 100 g
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7)	LEVOMENTHOL	5.7 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	6.3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
CALCIUM CARBONATE (UNII: H0G9379FGK)
STYRENE (UNII: 44LJ2U959V)
GLATIRAMER ACETATE (UNII: 5M691HL4BO)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
ZINC OXIDE (UNII: SOI2LOH54Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-385-20	20 in 1 BOX
1		2.0 g in 1 PATCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	11/26/2013

Labeler - United Exchange Corp. (840130579)