DR GOLDSONS- menthol, methyl salicylatw cream

DR GOLDSONS by

Drug Labeling and Warnings

DR GOLDSONS by is a Otc medication manufactured, distributed, or labeled by Inspec Solutions LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Menthol 8%

Methyl Salicylate 30%

PURPOSE

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

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

INDICATIONS & USAGE

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

Warnings

For external use only

Do not use

- on wounds or damaged skin

- with heating pad

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION

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

Curcuma Longa (Turmeric) Root Extract

DEA-Cetyl Phosphate

Glyceryl Stearate

Glycerin

Lanolin

Potassium Stearate

Stearic Acid

Water

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

DR GOLDSONS 
menthol, methyl salicylatw cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72667-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	8 g  in 100 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	30 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM STEARATE (UNII: 17V812XK50)
CURCUMA LONGA LEAF (UNII: H2HC4RY52C)
CETYL PHOSPHATE (UNII: VT07D6X67O)
GLYCERIN (UNII: PDC6A3C0OX)
LANOLIN (UNII: 7EV65EAW6H)
STEARIC ACID (UNII: 4ELV7Z65AP)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72667-009-01	113.4 mL in 1 JAR; Type 0: Not a Combination Product	04/17/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	03/21/2019

Labeler - Inspec Solutions LLC. (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions LLC.		081030372	manufacture(72667-009)