Label at a glance#

ProductULTRA STRENGTH PAIN RELIEF BALM

Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)

Label structure12 sections

Storage and handling

Other information This product may cause allergic reaction in some individuals. Test on small area before use.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purpose

Camphor 11%........................................................ Topical analgesic

Menthol 11%.......................................................... Topical analgesic

OTC - PURPOSE SECTION

Uses

For temporary relief of minor aches and pains of muscles and joints associated with over-exertion, simple backache, arhtritis, strains, and sprains.

WARNINGS SECTION

Warnings

For external use only.

OTC - WHEN USING SECTION

When using this product

Avoid contact with the eyes and mucous membranes
Do not apply to open wounds or damaged skin
Do not bandage or use heating pad

OTC - STOP USE SECTION

Stop use and ask a doctor if

Condition worsens
Severe skin irritation occurs
Pain persists for more than seven days
Pain clears up and then recurs a few days later

PREGNANCY SECTION

If pregnant or breast feeding, ask a healthcare professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed get medical help or contact a Poison Control Center immediately.

INDICATIONS & USAGE SECTION

Directions

Rub well on the affected area. Repeat 3 to 4 times dailys.
For children 2-12 years, consult a doctor before use.

STORAGE AND HANDLING SECTION

Other information

This product may cause allergic reaction in some individuals. Test on small area before use.

INACTIVE INGREDIENT SECTION

Inactive ingredients

cajuput oil, clove oil, dementholized mint oil, paraffin petrolatuma

DOSAGE & ADMINISTRATION SECTION

Distributed by:

MCURE HEALTH SOLUTIONS INC.

20819 Currier Rd #200

City of Industry, CA 91789

Made in China

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PAIN RELIEF BALM

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1089847	Camphor/Menthol (Topical)	camphor 0.11 MG/MG / menthol 0.11 MG/MG Topical Ointment	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1089847	camphor 11 % / menthol 11 % Topical Ointment	PSN	1
1089847	camphor 0.11 MG/MG / menthol 0.11 MG/MG Topical Ointment	SCD	1
1089847	camphor 11 % / menthol 11 % Topical Ointment	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71183-320-18	2020-01-31	C162847	48780-1	9d75b9d0-55a2-f424-e053-dadaa90a57ce	4a2aff23-e5a6-668f-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71183-320-18	ULTRA STRENGTH PAIN RELIEF BALM	18 g in 1 BOTTLE	OINTMENT	18		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71183-320	ULTRA STRENGTH PAIN RELIEF BALM (CAMPHOR MENTHOL OINTMENT) OINTMENT [SUZHOU VASTECH MEDICAL TECHNOLOGY CO., LTD]	1	Legacy NDC, 1 package rows	20170321_4a2aff23-e5a6-668f-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

ULTRA STRENGTH PAIN RELIEF BALM
Camphor Menthol Ointment
MENTHOL
PETROLATUM
PARAFFIN
CAMPHOR (SYNTHETIC)
CAJUPUT OIL
CLOVE OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71183-320	71183-320-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MENTHOL	L7T10EIP3A	ACTIB
PETROLATUM	4T6H12BN9U	IACT
PARAFFIN	I9O0E3H2ZE	IACT
CAMPHOR (SYNTHETIC)	5TJD82A1ET	ACTIB
CAJUPUT OIL	J3TO6BUQ37	IACT
CLOVE OIL	578389D6D0	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
4a2aff23-e5a7-668f-e054-00144ff88e88			4a2aff23-e5a6-668f-e054-00144ff88e88	2017-03-20	Warnings	Exact identifier spl id: 4a2aff23-e5a7-668f-e054-00144ff88e88 spl set id: 4a2aff23-e5a6-668f-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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

ULTRA STRENGTH PAIN RELIEF BALM