MENCAINE OTC- lidocaine, menthol patch

Mencaine OTC by

Drug Labeling and Warnings

Mencaine OTC by is a Otc medication manufactured, distributed, or labeled by Neptune Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients (in each patch):

Lidocaine 4%

Menthol 1%

Purpose

External Anesthetic

External Analgesic

USES

For temporary relief of pain

WARNINGS

For external use only.

Do not use:

More than 1 patch at a time
On wounds or damaged skin
For more than one week without consulting a doctor
If you are allergic to any ingredients of this product

When using this product:

Use only as directed
Avoid contact with the eyes, mucous membranes or rashes
Do not bandage tightly

Stop use and consult your physician if:

Localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering
Conditions worsen Symptoms persist for more than 7 days
Symptoms clear up and occur again within a few days

If pregnant or breast-feeding,

Ask a health 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 12 years and over:
Clean and dry affected area
Remove film from patch and apply to the skin
Apply 1 patch at a time to affected area, not more than 3 to 4 times daily
Remove patch from the skin after at most 8-hour application.
Children under 12 years of age:
Consult a doctor

Other information:

Store at 68-77°F (20-25°C)
Store in a cool dry place away from direct sunlight

Inactive ingredients:

Dihydroxyaluminium Aminoacetate, Edetate Disodium, Glycerin, Hydroxyacetophenone, Kaolin, L(+)-Tartaric Acid, Mineral oil, Polysorbate 80, Polyacrylic Acid, Polyvinylpyrrolidone K90, Propylene Glycol, Sodium Polyacrylate, Titanium Dioxide, Water

Questions or Comments:

info@neptuneice.cool

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MENCAINE OTC 
lidocaine, menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72594-1002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 mg  in 100 mg
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
MINERAL OIL (UNII: T5L8T28FGP)
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TARTARIC ACID (UNII: W4888I119H)
WATER (UNII: 059QF0KO0R)
KAOLIN (UNII: 24H4NWX5CO)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
PVP (UNII: FZ989GH94E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72594-1002-1	5 in 1 BOX	12/31/2024
1		3 in 1 POUCH
1		8500 mg in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/31/2024

Labeler - Neptune Products (081502369)