Herbalgy

Manufacturer
Herbalgy Pharmaceutical Limited
Effective date
2012-02-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:31:09

Label at a glance#

ProductHerbalgy
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
Methyl Salicylate 31.5%
Menthol 16%
Camphor 10%

OTC - PURPOSE SECTION

Purpose
External Analgesic
External Analgesic
External Analgesic

INDICATIONS & USAGE SECTION

Uses: For the temporary relief of minor aches and pains of muscles and joints associated withsimple backache, strains, bruises and sprains.

WARNINGS SECTION

Warnings: FOR EXTERNAL USE ONLY

OTC - DO NOT USE SECTION

Do not use
  • Apply on wounds, irritated or damaged skin.
  • Otherwise than as directed

OTC - WHEN USING SECTION

When using this product
  • Avoid contact with the eyes, mouth or mucous membranes.
  • Do not bandage tightly.

OTC - STOP USE SECTION

Stop use and ask a doctor if:
  • Condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days.
  • Excessive irritation of the skin develops.
  • When using this product for arthritis: Pain persists for more than 10 days, redness is present or in conditions affecting children under 12 years of age

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast feeding, see the advise of a health professional before using this product.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental poisoning. If swallowed, contact a Doctor or Poison Control Center immediately

DOSAGE & ADMINISTRATION SECTION

Directions
Adults and children2 years of age and older: Apply to affected area not more than 3-4 times daily.
Children under 2 years of age: Do not use, consult a doctor

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Eucalyptus oil, Olibanum, Myrhha resins, Corydalis rhizome and Drynaria fortunei extracts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label
image of package label
image of package label


DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1247969camphor 10 % / menthol 16 % / methyl salicylate 31.5 % Topical OilPSN1
1247974HERBALGY 10 % / 16 % / 31.5 % Topical OilPSN1
1247974camphor 100 MG/ML / menthol 160 MG/ML / methyl salicylate 315 MG/ML Topical Oil [Herbalgy]SBD1
1247969camphor 100 MG/ML / menthol 160 MG/ML / methyl salicylate 315 MG/ML Topical OilSCD1
1247969camphor 10 % / menthol 16 % / methyl salicylate 31.5 % Topical OilSY1
1247974Herbalgy (camphor 10 % / menthol 16 % / methyl salicylate 31.5 % ) Topical OilSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66898-100-502020-01-31C16284748780-19d75b9d0-983e-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66898-100-50Herbalgy50 mL in 1 BOTTLE, GLASSOIL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66898-100HERBALGY (CAMPHOR MENTHOL METHYL SALICYLATE) OIL [HERBALGY PHARMACEUTICAL LIMITED ]1Legacy NDC, 1 package rows20120315_2a04bcad-d8eb-4b76-8c7c-15b73ec8b77a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ET1
MENTHOLACTIVE INGREDIENTL7T10EIP3A1
METHYL SALICYLATEACTIVE INGREDIENTLAV5U5022Y1
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ET1
MENTHOLACTIVE MOIETYL7T10EIP3A1
METHYL SALICYLATEACTIVE MOIETYLAV5U5022Y1
CORYDALIS YANHUSUO TUBERINACTIVE INGREDIENT0TUP42692Z1
DRYNARIA FORTUNEI ROOTINACTIVE INGREDIENT731W842X8Q1
EUCALYPTUS OILINACTIVE INGREDIENT2R04ONI6621
FRANKINCENSEINACTIVE INGREDIENTR9XLF1R1WM1
MYRRHINACTIVE INGREDIENTJC71GJ1F3L1

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66898-10066898-100-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 1 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
EUCALYPTUS OILEUCALYPTUS OIL2R04ONI662SYRUP / ORALNAExact identifier — unii candidate

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
efcea474-f352-4b6f-8859-f9faece1f41f2a04bcad-d8eb-4b76-8c7c-15b73ec8b77a2012-02-27WarningsExact identifier
spl id: efcea474-f352-4b6f-8859-f9faece1f41f
spl set id: 2a04bcad-d8eb-4b76-8c7c-15b73ec8b77a

Reported adverse events (FAERS/openFDA)#

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