FDA.reportPublic FDA data

Bio-Relief

Manufacturer
Scientific Solutions Global LLC
Effective date
2020-02-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:03:45

Label at a glance#

ProductBio-Relief
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

For external use only. Flammable, keep away from fire/flame.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children, if swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Adults & children 2 yrs of age and older: Apply to affected area not more than 4 times daily in one direction, not circular. Children under 2 years of age, consult a physician. Massage not necessary. Shake well before use.

INACTIVE INGREDIENT SECTION

Aloe Vera Oil, Arnica Flower Tincture, Boswellia Powder, Camphor, Frankincense Oil, Green Tea, Hydroxypropyl Cellulose NF, Isopropyl Alcohol, Lavender Oil, Propylene Glycol, Tea Tree Oil, Thymol, Vitamin E.

OTHER SAFETY INFORMATION

Store in a cool and dry place with lid closed tightly.

Questions or Comments? E-mail: info@scisolglobal.com Manufactured and Distributed by: Scientific Solutions Global LLC, Carle Place, NY, USA

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
259249menthol 10 % Topical GelPSN1
259249menthol 0.1 MG/MG Topical GelSCD1
259249menthol 10 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71718-200-012021-07-23C16284748780-1c7ccaba7-282f-fd44-e053-dadaa90aa01b9e541811-0a2d-310f-e053-2a95a90ad5b0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71718-200-01Bio-Relief89 mL in 1 BOTTLEGEL891

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71718-200BIO-RELIEF (MENTHOL) GEL [SCIENTIFIC SOLUTIONS GLOBAL LLC]1Legacy NDC, 1 package rows20200214_9e541811-0a2d-310f-e053-2a95a90ad5b0.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71718-20071718-200-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL ALCOHOLND2M416302IACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
LAVENDER OILZBP1YXW0H8IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIED9XZ8H6N6OHIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
ARNICA MONTANAO80TY208ZWIACT
ALPHA-TOCOPHEROLH4N855PNZ1IACT
TEA TREE OILVIF565UC2GIACT
ALOE VERA LEAFZY81Z83H0XIACT
THYMOL3J50XA376EIACT

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
9e541811-0a2e-310f-e053-2a95a90ad5b09e541811-0a2d-310f-e053-2a95a90ad5b02020-02-11WarningsExact identifier
spl id: 9e541811-0a2e-310f-e053-2a95a90ad5b0
spl set id: 9e541811-0a2d-310f-e053-2a95a90ad5b0

Reported adverse events (FAERS/openFDA)#

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