BL3 Mineral Ice Gel

Manufacturer
Inspec Solutions, LLC.
Effective date
2019-06-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:20:47

Label at a glance#

ProductBL3 Mineral Ice Gel
Active ingredientMENTHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Menthol 2%

OTC - PURPOSE SECTION

Menthol 2% .........................Analgesic

INDICATIONS & USAGE SECTION

Uses

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

WARNINGS SECTION

Warnings

For external use only

• sue only as directed

• avoid contact with eyes

• do not bandage tightly

• do not apply to wounds or damaged skin

•​ do not use with heating pad

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days.

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

Direction

• For adult & children 2 years of age and older

• Cleans ad dry skin

• Apply to affected area not more than 3 to 4 times daily

• may be used with wet or dry bandages in conjunction with ice packs

• children under 2 years of age, consult a doctor

INACTIVE INGREDIENT SECTION

Inactive Ingredients Ammonium Hydroxide, Carbomer, Cupric Sulfate, FD&C Blue No. 1, Isopropyl Alcohol, Magnesium Sulfate, Sodium Hydroxide, Thymol, Water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BL3 Ice GelBL3 Ice Gel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72667-013-012021-01-29C16284748780-1ba0f9c33-4587-a910-e053-dadaa90a0b85THERAPEUTIC MENTHOL GEL

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72667-01372667-013-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
8b4adae1-005f-13a5-e053-2995a90a3b888b233916-6579-e23d-e053-2a95a90a13f12019-06-14WarningsExact identifier
spl id: 8b4adae1-005f-13a5-e053-2995a90a3b88
spl set id: 8b233916-6579-e23d-e053-2a95a90a13f1

Reported adverse events (FAERS/openFDA)#

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