Pain Relief Herbal balm

Manufacturer
Albert Max, Inc.
Effective date
2018-12-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:39:35

Label at a glance#

ProductPain Relief Herbal balm
Active ingredientMETHYL SALICYLATE, MENTHOL, UNSPECIFIED FORM, CAMPHOR (NATURAL)
Label structure11 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints due to: •arthritis •strains •bruises •sprains •simple backache

Dosage and administration

• Apply to the affected area. Rub well on affected area. • Repeat 2 times daily. • Children under 2 years of age: Do not use or consult a doctor.

Storage and handling

•Store at room temperature, 20 to 25° C(68 to 77° F)

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Methyl Salicylate 20.7%

Menthol 15.6%

Camphor 3.1%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints due to:
•arthritis •strains •bruises •sprains •simple backache

Warnings

WARNINGS SECTION

For external use only

Do not use

•on wounds •irritated or damaged skin •sensitive skin

•with a heating pad •if pregnant

•with, or as the same time as, other external analgesic products

•if allergic to aspirin or salicylates

•if allergic to any ingredients of this product

When using this product

•avoid contact with the eyes •do not bandage tightly

•do not apply to wounds or damaged skin

•do not use 1 hour before or after bathing

Stop use and ask a doctor if

•condition worsens •symptoms persist for more than 7 days

•symptoms clear up and occur again within a few days

•excessive irritation of the skin develops

•redness is present  •side effects occur.

If pregnant, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental poisoning.
In case of overdose, get medical help or contact a Poison Control Center right away.
Do not use otherwise than as directed.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply to the affected area. Rub well on affected area.
• Repeat 2 times daily.
• Children under 2 years of age: Do not use or consult a doctor.

Other Information

STORAGE AND HANDLING SECTION

•Store at room temperature, 20 to 25° C(68 to 77° F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Eucalyptus oil, Lavender oil, Vaseline, White beeswax

Question or Comments?

OTC - QUESTIONS SECTION

1-888-811-1133

SPL UNCLASSIFIED SECTION

Distributed by: America Health Herbs, Inc. 15361 Brookhurst #104 Westminster, CA 93683 USA 

Relieves Pain Herbal Essence Ultra Strength

MADE IN TAIWAN

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68233-807-012023-10-10C16284748780-1d6a99b39-b86f-a426-e053-dadaa90af4c2PAIN RELIEF HERBAL BALM
68233-807-012022-01-28C16284748780-1d6a99b39-b86f-a426-e053-dadaa90af4c2PAIN RELIEF HERBAL BALM

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68233-80768233-807-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
07574155-0fb3-d615-e063-6394a90acaaf36328985-ba41-4c8a-8a73-2bb813a830d72023-10-10WarningsExact identifier
spl set id: 36328985-ba41-4c8a-8a73-2bb813a830d7

Reported adverse events (FAERS/openFDA)#

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