NEUROFLEX TOPICAL PAIN RELIEVING LIQUID (camphor- synthetic, menthol solution

NEUROFLEX Topical Pain Relieving Liquid by

Drug Labeling and Warnings

NEUROFLEX Topical Pain Relieving Liquid by is a Otc medication manufactured, distributed, or labeled by Almark Products Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active Ingredients

Camphor 3.00% Menthol 2.00%

Purpose

Pain Reliever

Uses

For temporary relief of minor aches and pains of muscles and joints: arthritis simple backaches soreness  strains sprains bruises

Warnings

For External Use Only

Flammable: Keep away from fire or flame.

Do not use

on wounds on damaged skin  on mucous membranes

When using this product

avoid contact with eyes  do not bandage tightly do not use a heating pad

Stop use and ask a doctor if

condition worsens  symptoms persist for more than 7 days  symptoms clear up and occur again within a few days

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 of age and older. Apply to affected areas not more than 3 to 4 times daily. No need to rub in. Children under 2 years of age: Consult a physician.

Inactive Ingredients

Eucalyptus Globulus Lead (Eucaluptus) Oil, Melaleuca, Alternifolia (australian Tea Tree) Leaf Oil, Pinus Sylvestris (Pine) Oil, Polysorbate-20, SD-Alcohol 40B.

Package Labeling:

INGREDIENTS AND APPEARANCE

NEUROFLEX TOPICAL PAIN RELIEVING LIQUID 
camphor (synthetic), menthol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69876-1740
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	30 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
EUCALYPTUS GUM (UNII: 72T9EZC2VX)
TEA TREE OIL (UNII: VIF565UC2G)
PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69876-1740-0	118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/01/2021

Labeler - Almark Products Inc (961410933)