BioFlexor

Manufacturer
Health Care Laboratories Inc.
Effective date
2014-05-21
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 22:40:26

Label at a glance#

ProductBioFlexor
Active ingredientMENTHOL
Label structure10 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Apply BioFlexor gel onto the affected area(s) up to 3 to 4 times daily as needed.  Apply sufficient amount at bedtime for a restful sleep and in the morning to loosen stiff muscles and joints, and reduce pain.  The therapeutic effects of BioFlexor will allow you to become more active and return to normal activities of daily living.

WARNINGS SECTION

For External use only.  Do not swallow.  If Accidentally ingested, induce vomiting.  Call a physician or poison control center immediately.  If irritation develops, discontinue use of this product and consult a physician.  Do not use on open sores, wounds, irritated or broken skin.  Do not use with other creams, gels, ointments, topical medications, heating pads or other heat producing devices.  Avoid contact with eyes or mucous membrane.  Store in a cool dry place.  Keep out of reach of children to avoid accidental poisoning. BioFlexor gel is contraindicated in patients with a known hypersensitivity to menthol.  For children under 2, pregnant or nursing mothers, consult a physician. 



HOW SUPPLIED SECTION

0.25 oz (7.5 Gm) Jars NDC# 62391-001-10
2.25 oz (67.5 Gm) Jars NDC# 62391-001-02
4.5 oz (135 Gm) Jars NDC# 62391-001-04
32 oz (960 Gm) Jars NDC# 62391-001-30

TO PLACE ORDERS:
To place orders, please call customer service at:
1-800-909-9854
Or Fax orders to:
1-800-316-7853

Visit our website at:
www.bioflexor.com

Mfg. by HEALTH CARE LABS, INC.
P.O. Box 1734, Cleveland, TX 77328

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

SPL PATIENT PACKAGE INSERT SECTION

BioFlexor®
Deep Penetrating
Effective Pain Relief Gel

Description:  BioFlexor® gel is an OTC topical analgesic preparation which delivers deep penetrating, effective pain relief.  BioFlexor® is a unique product from several viewpoints.  In developing BioFlexor®, our main focus was to formulate a potent topical analgesic agent that would minimize the need for oral narcotic analgesics.  The result is an exceptional product that truly helps those individuals suffering from the pain associated with the spectrum of medical conditions from arthritis to muscle aches and pain, simple back aches, strains, bruises, and sprains.  Menthol is the only listed active ingredient on the BioFlexor® label.  The other all natural components work synergistically to produce the pain relieving activity.  Another unique aspect of BioFlexor® relates to the immediate and long-lasting pain relief without the side effects of lingering scent (Methyl Salicylate rubs, ie. Ben Gay), burning sensation (Capsaicin ie. Zostrix, Theragesic, Icy-Hot), greasy residue (ie. Aspercreme, Ben-Gay), and dry skin (alcohol formulations, ie. Biofreeze).  The BioFlexor® formulation contains no alcohol, capsaicin, or methyl salicylate.

Mechanism of Action:  The initial pain relief mechanism produced by the absorption of BioFlexor® generates a topical cooling effect.  This is a result of vasoconstriction of peripheral vessels in the affected areas, yielding a decreased blood flow.  This action causes a decrease in temperature of the skin and subcutaneous tissues.  As penetration continues, an interruption of sympathetic nerve conduction occurs, producing a warm vasodilation.  This in turn increases the blood flow to muscle tissues and to the surface of the skin, promoting the healing process and rendering analgesic properties.  BioFlexor® gel is contraindicated in patients with a known hypersensitivity to menthol.

How Supplied:                                       
2.25oz (67.5gm) Jars…..NDC# 62391-001-02                     
4.5oz (135gm) Jars …..…NDC# 62391-001-04     

TO PLACE ORDERS:
Please call Customer Service at:   1-800-909-9854 
or Fax Orders to:    1-800-316-7853
or Visit our Website at:   www.bioflexor.com       

Mfg. By: HEALTH CARE LABORATORIES, INC.               
112 S. COLLEGE AVE. #100A
CLEVELAND, TX 77327
Store at controlled room temperature 15˚-30˚C (59˚-86˚F)    
 *Registered trademarks are the property of their respective owners.                

DRUG FACTS
Active Ingredient     Purpose
Menthol 3%,           Topical Analgesic
Uses 
Temporarily relieves the minor aches and pains of muscles and joints associated with:
•simple backache •arthritis •strains •bruises •sprains
Warnings
For external use only.
Do Not Use:
• on wounds or damaged skin
• with a heating pad
• on a child under 12 years of age with arthritis-like conditions
Ask a doctor before use if you have redness over the affected area.
When using this product:
• avoid contact with the eyes or mucous membranes
• do not bandage tightly
Stop use and ask a doctor if:
• condition worsens or symptoms persist for more than 7 days
• symptoms clear up and occur again within a few days
• excessive skin irritation occurs
Keep out of reach of children.
If swallowed, get medical help or contact the Poison Control Center right away.
Directions
Adults and children 12 years of age and older:
• apply to affected area not more than 3 to 4 times daily.
Children under 12 years of age:
• consult a doctor
Other Information
• Store at 20°-25°C (68°-77°)
• Lot No. and Expiration Date:  See Container
Inactive Ingredients
Carbopolymer, Edetate Disodium Peacock Blue MX26,
Phenoxyethanol/Paraben Blend, Polysorbate 20, Potassium Sorbate,
Proprietary Blend, Purified Water, Sodium Hydroxide

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:  Menthol 3%

INACTIVE INGREDIENT SECTION

Inactive Ingredients:  Carbopol Polymer, Edetate Disodium, Peacock Blue MX26, Phenoxyethanol/Paraben Blend, Polysorbate 20, Potassium Sorbate, Proprietary Blend, Purified Water, Sodium Hydroxide

OTC - PURPOSE SECTION

Description:  BioFlexor® gel is an OTC topical analgesic preparation which delivers deep penetrating, effective pain relief.  BioFlexor® is a unique product from several viewpoints.  In developing BioFlexor®, our main focus was to formulate a potent topical analgesic agent that would minimize the need for oral narcotic analgesics.  The result is an exceptional product that truly helps those individuals suffering from the pain associated with the spectrum of medical conditions from arthritis to muscle aches and pain, simple back aches, strains, bruises, and sprains.  Menthol is the only listed active ingredient on the BioFlexor® label.  The other all natural components work synergistically to produce the pain relieving activity.  Another unique aspect of BioFlexor® relates to the immediate and long-lasting pain relief without the side effects of lingering scent (Methyl Salicylate rubs, ie. Ben Gay), burning sensation (Capsaicin ie. Zostrix, Theragesic, Icy-Hot), greasy residue (ie. Aspercreme, Ben-Gay), and dry skin (alcohol formulations, ie. Biofreeze).

The BioFlexor formulation contains no alcohol, capsaicin or methyl salicylate.

INDICATIONS & USAGE SECTION

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

USAGE:  Adults and children 12 years of age and older:  Apply to affected area not more than 3 to 4 times daily.  Children under 12 years of age, pregnant or nursing mothers:  Consult a physician.

BioFlexor Jar

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1304408BioFlexor 3 % Topical GelPSN5
259150menthol 3 % Topical GelPSN5
1304408menthol 0.03 MG/MG Topical Gel [Bioflexor]SBD5
259150menthol 0.03 MG/MG Topical GelSCD5
1304408Bioflexor 0.03 MG/MG Topical GelSY5
1304408Bioflexor 3 % Topical GelSY5
259150menthol 3 % Topical GelSY5

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62391-001-02BioFlexor67.5 g in 1 JARGEL67.55
62391-001-04BioFlexor135 g in 1 JARGEL1355
62391-001-10BioFlexor7.5 g in 1 JARGEL7.55
62391-001-30BioFlexor960 g in 1 JARGEL9605

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62391-001BIOFLEXOR (MENTHOL) GEL [HEALTH CARE LABORATORIES INC.]5Legacy NDC, 4 package rows20141003_455353d1-74dc-4b54-9da8-9ab5b81d14be.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62391-001-02GM - Gram62391-00134430c44-6615-4c39-9bbf-7af29105ec1b12015-10-02
62391-001-04GM - Gram62391-001cdccd0e3-e38a-48dc-963c-d43b49002f5512015-10-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
MENTHOLACTIVE INGREDIENTL7T10EIP3A5
MENTHOLACTIVE MOIETYL7T10EIP3A5
WATERINACTIVE INGREDIENT059QF0KO0R5

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62391-00162391-001-04, 62391-001-02, 62391-001-10, 62391-001-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
WATER059QF0KO0RIACT

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
0b669957-1ea3-45ff-83a4-851ee52b5e51455353d1-74dc-4b54-9da8-9ab5b81d14be2014-05-21WarningsExact identifier
spl id: 0b669957-1ea3-45ff-83a4-851ee52b5e51
spl set id: 455353d1-74dc-4b54-9da8-9ab5b81d14be

Reported adverse events (FAERS/openFDA)#

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