Active ingredients Purpose

Camphor – 4.00%                                Topical Analgesic
Menthol – 10.00%                           Topical Analgesic
Methyl Salicylate – 30.00%                Topical Analgesic

Uses

temporarily relieves minor pain associated with:
arthritis
simple backache
muscle strains
bruises
muscle sprains

Warnings

For external use only

Flammable

• keep away from fire or flame. • avoid long term
storage above 104˚F. • do not puncture or incinerate. Contents under
pressure. • do not store at temperatures above 120˚F

• do not use while smoking or near heat or flame
• avoid long term storage above 104F
• do not puncture or incinerate. Contents under pressure
• do not store at temperature above 120F

When using this product

• avoid contact with eyes and mucous membranes
• do not apply to wounds or damages skin
• do not bandage tightly or use with a heating pad
• use only as directed

Stop use and ask a doctor if

• condition worsens
• symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of the children

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

If pregnant or breast-feeding, ask a health professional before use

Directions

• shake well
• adults and children 2 years of age and older: spray on affected area, not more than 3 to 4 times daily
• children under 2 years of age: consult a doctor

Inactive ingredients

Alcohol Denat.

image description

ULTRA STRENGTH PAIN RELIEF
camphor 4%, menthol 10%, methyl salicylate 30% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:41520-317
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	4 g in 100 mL
Menthol (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	Menthol	10 g in 100 mL
Methyl Salicylate (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	Methyl Salicylate	30 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:41520-317-00	118 mL in 1 CAN; Type 0: Not a Combination Product	08/26/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	08/26/2014

Labeler - Car One (809183973)

Registrant - Product Quest Mfg (927768135)

Name	Address	ID/FEI	Business Operations
Establishment
Product Quest Mfg		927768135	manufacture(41520-317) , label(41520-317)

Drug Facts