MENTHOLATUM DEEP HEATING RUB EXTRA STRENGTH- menthol, methyl salicylate cream

Mentholatum Deep Heating Rub by

Drug Labeling and Warnings

Mentholatum Deep Heating Rub by is a Otc medication manufactured, distributed, or labeled by The Mentholatum Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Menthol 8%

Methyl salicylate 30%

Purpose

Menthol - External analgesic

Methyl salicylate - External analgesic

Uses

temporarily relieves minor aches and pains of muscles and joints due to

• arthritis
• strains
• simple backache
• sprains

Warnings

For external use only

When using this product

• use only as directed
• do not get into eyes or on mucous membranes
• do not apply to wounds or damaged skin
• do not bandage tightly
• do not use with heating pad, other heat sources, or right after a shower/bath
• do not use in combination with other external analgesic products

Stop use and ask a doctor if

• condition worsens
• excessive irritation, burning, or discomfort of the skin develops
• symptoms persist for more than 7 days or clear up and occur again within a few days

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

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• adults and children 2 years and over: apply to affected area not more than 3 to 4 times daily
• children under 2 years: ask a doctor

Inactive ingredients

glyceryl stearate, isoceteh-20, poloxamer 407, purified water, sodium lauryl sulfate, sorbitan stearate

Questions?

1-877-636-2677 MON-FRI 9 AM to 5 PM (EST)

www.mentholatum.com

Package/Label Principal Display Panel

INGREDIENTS AND APPEARANCE

MENTHOLATUM DEEP HEATING RUB  EXTRA STRENGTH
menthol, methyl salicylate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10742-2002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	80 mg  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	300 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
POLOXAMER 407 (UNII: TUF2IVW3M2)
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10742-2002-4	2 in 1 CARTON	12/15/1992
1		57 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	12/15/1992

Labeler - The Mentholatum Company (002105757)