Ultra Strength Pain Relief

Manufacturer: Product Quest Mfg
Effective date: 2018-06-25
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:56:03

Label at a glance#

ProductUltra Strength Pain Relief

Active ingredientCAMPHOR (SYNTHETIC), Menthol, Methyl Salicylate

Label structure8 sections

Indications and uses

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

Dosage and administration

• 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

Label contents#

Full prescribing information#

Active ingredients Purpose

OTC - ACTIVE INGREDIENT SECTION

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

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

Flammable

SPL UNCLASSIFIED SECTION

• 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

OTC - WHEN USING SECTION

• 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

OTC - STOP USE SECTION

• 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• 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

INACTIVE INGREDIENT SECTION

Alcohol Denat.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1600127	camphor 4 % / menthol 10 % / methyl salicylate 30 % Topical Spray	PSN	1
1600127	camphor 40 MG/ML / menthol 100 MG/ML / methyl salicylate 300 MG/ML Topical Spray	SCD	1
1600127	camphor 4 % / menthol 10 % / methyl salicylate 30 % Topical Spray	SY	1

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0727510004426	GTIN-13: 0727510004426 EAN-13: 0727510004426 GTIN-12: 727510004426 UPC-A: 727510004426 GTIN storage (14 digits): 00727510004426	label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64048-5114-4	2020-01-31	C162847	48780-1	9d75b9d0-d633-f424-e053-dadaa90a57ce	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64048-5114-4	Ultra Strength Pain Relief	113 g in 1 CAN	SPRAY	113		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64048-5114	ULTRA STRENGTH PAIN RELIEF (CAMPHOR 4%, MENTHOL 10%, METHYL SALICYLATE 30%) SPRAY [PRODUCT QUEST MFG]	1	Legacy NDC, 1 package rows	20180625_4a595401-20af-437e-a658-44e9358d9008.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

Ultra Strength Pain Relief
Camphor 4%, Menthol 10%, Methyl Salicylate 30%
CAMPHOR (SYNTHETIC)
Menthol
Methyl Salicylate
SALICYLIC ACID
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64048-5114	64048-5114-4

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CAMPHOR (SYNTHETIC)	5TJD82A1ET	ACTIB
Menthol	L7T10EIP3A	ACTIB
Methyl Salicylate	LAV5U5022Y	ACTIB
ALCOHOL	3K9958V90M	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2c4c25cc-4283-435e-a614-1cad8d1338f6			4a595401-20af-437e-a658-44e9358d9008	2018-06-25	Warnings	Exact identifier spl id: 2c4c25cc-4283-435e-a614-1cad8d1338f6 spl set id: 4a595401-20af-437e-a658-44e9358d9008

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.