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

Ultra Strength Pain Relief by

Drug Labeling and Warnings

Ultra Strength Pain Relief by is a Otc medication manufactured, distributed, or labeled by Product Quest Mfg. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients                             Purpose

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

PURPOSE

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64048-5114
Route of Administration	TOPICAL

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64048-5114-4	113 g in 1 CAN; Type 0: Not a Combination Product	02/06/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	02/06/2014

Labeler - Product Quest Mfg (927768135)

Registrant - Product Quest Mfg (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg		927768135	manufacture(64048-5114) , label(64048-5114)