NERVE REVERSE PAIN RELIEF- menthol cream

NERVE REVERSE PAIN RELIEF by

Drug Labeling and Warnings

NERVE REVERSE PAIN RELIEF by is a Otc medication manufactured, distributed, or labeled by Pogue Medical Services. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient:

Menthol 4.00%

Purpose

Topical Analgesic

Use

• For the temporary relief of minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and strains.

Warnings:

• For external use only.
• Avoid contact with eyes.
• If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children.

• If swallowed, consult physician.
• Do not bandage tightly.

If pregnant or breast feeding, 

contact physician prior to use.

Directions

Adults and children two-years of age or older: Apply to affected area not more than three to four times daily.

• Children under two-years of age: consult a physician.

Additional Information:

Store at room temperature.

Other Ingredients:

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), l-Arginine, Biotin, Boswellia Serrata Extract, Carbomer, l-Carnitine, Ethylhexylglycerin, Eucalyptus Globulus Oil, Glyceryl Stearate, Lanolin, a-Lipoic Acid, Methylsulfonylmethane (MSM), Pantothenic Acid (Vitamin B5), Phenoxyethanol, Polysorbate-20, Riboflavin (Vitamin B2), Ricinus Comminis (Castor) Oil, SD-Alcohol 40B, Stearic Acid, Thiamine (Vitamin B1), Tocopheryl Acetate (Vitamin E), Triethanolamine.

Package Labeling:

INGREDIENTS AND APPEARANCE

NERVE REVERSE PAIN RELIEF 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73067-870
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ARGININE (UNII: 94ZLA3W45F)
BIOTIN (UNII: 6SO6U10H04)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
LEVOCARNITINE (UNII: 0G389FZZ9M)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
EUCALYPTUS OIL (UNII: 2R04ONI662)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
LANOLIN (UNII: 7EV65EAW6H)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
PANTOTHENIC ACID (UNII: 19F5HK2737)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
RIBOFLAVIN (UNII: TLM2976OFR)
STEARIC ACID (UNII: 4ELV7Z65AP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73067-870-04	118 mL in 1 JAR; Type 0: Not a Combination Product	04/15/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/15/2019

Labeler - Pogue Medical Services (085490789)