NEUROFLEX TOPICAL PAIN RELIEVING LIQUID- camphor (synthetic), menthol solution 
Almark Products Inc

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NEUROFLEX Topical Pain Relieving Liquid

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:

Label

NEUROFLEX TOPICAL PAIN RELIEVING LIQUID 
camphor (synthetic), menthol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69876-1740
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)30 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
EUCALYPTUS GUM (UNII: 72T9EZC2VX)  
TEA TREE OIL (UNII: VIF565UC2G)  
PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69876-1740-0118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01704/01/2021
Labeler - Almark Products Inc (961410933)

Revised: 11/2023
Document Id: 09d72589-142c-349f-e063-6294a90a4d95
Set id: 6da3aa84-7a01-4041-8792-a4bbf49e6e4e
Version: 2
Effective Time: 20231110
 
Almark Products Inc