PAIN RELIEF- dl-camphor, l-menthol, methyl salicylate patch patch

Pain Relief by

Drug Labeling and Warnings

Pain Relief by is a Otc medication manufactured, distributed, or labeled by Kareway Product, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

DL-Camphor 1.2%

L-Menthol 5.7%

Methyl Salicylate 6.3%

Purpose

Topical Analgesic

Topical Analgesic

Topical Analgesic

Uses

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

• arthritis
• simple backaches
• strains
• bruises
• sprains

Warnings

for external use only

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 a doctor before use,

if you are allergic to any ingredients of this product.

When using this product

• use only as directed
• avoid contact with eyes, mucous membranes or rashes
  

Stop use and ask a doctor 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.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 12 years of age and over:

• clean and dry affected area
• remove patch from film
• apply to affected area not more than 3 to 4 times daily for 7 days
• wear up to 8 hours per application

Children under 12 years of age:

• consult a doctor
  

Other information

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

Inactive ingredients

butylated hydroxytoluene, glyceryl rosinate, natural rubber, polybutene, polyisobutylene, precipitated calcium carbonate, quintone, sorbitan stearate, tocopherol acetate, ys resin, zinc oxide

Carton label

Pain Relief Patch

INGREDIENTS AND APPEARANCE

PAIN RELIEF 
dl-camphor, l-menthol, methyl salicylate patch patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67510-0305
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	0.4 mg
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7)	LEVOMENTHOL	1.8 mg
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	2 mg

Inactive Ingredients
Ingredient Name	Strength
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
CALCIUM CARBONATE (UNII: H0G9379FGK)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ZINC OXIDE (UNII: SOI2LOH54Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67510-0305-2	20 in 1 CARTON	01/25/2012
1		1 in 1 POUCH; 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	01/25/2012

Labeler - Kareway Product, Inc. (121840057)