NEUROFLEX Topical Pain Relieving Liquid

Manufacturer
Almark Products Inc
Effective date
2023-11-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:59:52

Label at a glance#

ProductNEUROFLEX Topical Pain Relieving Liquid
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL
Label structure6 sections

Indications and uses

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

Dosage and administration

• 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.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 3.00% Menthol 2.00%

Purpose

OTC - PURPOSE SECTION

Pain Reliever

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For External Use Only

Flammable: Keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

• on wounds • on damaged skin • on mucous membranes

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

• 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• 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

INACTIVE INGREDIENT SECTION

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

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2534165camphor 3 % / menthol 2 % Topical SolutionPSN2
2534165camphor 30 MG/ML / menthol 20 MG/ML Topical SolutionSCD2
2534165camphor 3 % / menthol 2 % Topical SolutionSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69876-1740-0NEUROFLEX Topical Pain Relieving Liquid118 mL in 1 BOTTLE, SPRAYSOLUTION1182

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69876-1740NEUROFLEX TOPICAL PAIN RELIEVING LIQUID (CAMPHOR (SYNTHETIC), MENTHOL) SOLUTION [ALMARK PRODUCTS INC]2Current NDC, Legacy NDC, 1 package rows20231111_6da3aa84-7a01-4041-8792-a4bbf49e6e4e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69876-174069876-1740-0

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NEUROFLEX Topical Pain Relieving LiquidCAMPHOR (SYNTHETIC), MENTHOLAlmark Products Inc6da3aa84-7a01-4041-8792-a4bbf49e6e4e2023-11-10WarningsExact identifier
ndc (package): 69876-1740-0
ndc (product): 69876-1740
ndc11 (package): 69876174000
spl id: 09d72589-142c-349f-e063-6294a90a4d95
spl set id: 6da3aa84-7a01-4041-8792-a4bbf49e6e4e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.