FDA.reportPublic FDA data

DR GOLDSON'S PAIN CREAM

Manufacturer
Inspec Solutions LLC.
Effective date
2019-03-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:25:42

Label at a glance#

ProductDR GOLDSONS
Active ingredientMENTHOL, METHYL SALICYLATE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Menthol 8%

Methyl Salicylate 30%

OTC - PURPOSE SECTION

Menthol 8% ...............................External Analgesic

Methyl Salicylate 30% ...............External Analgesic

INDICATIONS & USAGE SECTION

INDICATIONS & USAGE SECTION

Uses for temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains.

WARNINGS SECTION

Warnings

For external use only

Do not use

- on wounds or damaged skin

- with heating pad

OTC - STOP USE SECTION

Stop use and ask a doctor if

- condition worsens or symptoms persist for more than 7 days

- symptoms clear up and occur again within a few days

- excessive skin irritation occurs

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.

DOSAGE & ADMINISTRATION SECTION

Direction

- Use only as directed

- Adults and children over 12 years: Apply to affected area no more than 3 to 4 times daily.

- Children 12 years or younger: ask a doctor.

- Close cap tightly after use.

INACTIVE INGREDIENT SECTION

Curcuma Longa (Turmeric) Root Extract

DEA-Cetyl Phosphate

Glyceryl Stearate

Glycerin

Lanolin

Potassium Stearate

Stearic Acid

Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DR GOLDSON'SDR GOLDSON'S
​
​

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72667-009-012021-01-29C16284748780-1ba0f9c33-4f01-a910-e053-dadaa90a0b85DR GOLDSON'S PAIN CREAM

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72667-009DR GOLDSONS (MENTHOL, METHYL SALICYLATW) CREAM [INSPEC SOLUTIONS LLC.]1Legacy NDC20190418_84a10bf8-ff0a-7108-e053-2a91aa0a9ebb.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72667-00972667-009-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
POTASSIUM STEARATE17V812XK50IACT
MENTHOLL7T10EIP3AACTIB
METHYL SALICYLATELAV5U5022YACTIB
CURCUMA LONGA LEAFH2HC4RY52CIACT
CETYL PHOSPHATEVT07D6X67OIACT
GLYCERINPDC6A3C0OXIACT
LANOLIN7EV65EAW6HIACT
STEARIC ACID4ELV7Z65APIACT
WATER059QF0KO0RIACT

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
49ebd3e1-74f2-df36-e063-6394a90abaf784a10bf8-ff0a-7108-e053-2a91aa0a9ebb2026-02-03WarningsExact identifier
spl set id: 84a10bf8-ff0a-7108-e053-2a91aa0a9ebb

Reported adverse events (FAERS/openFDA)#

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