BLACK ICE MEDICATED PATCHES

Manufacturer
Carbon Biotech Llc
Effective date
2018-07-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:56:25

Label at a glance#

ProductBLACK ICE MEDICATED PATCHES
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure9 sections

Indications and uses

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

Dosage and administration

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: Consult a doctor. Clean skin of oil, dirt, lotions, etc. and dry completely before use. If necessary, use medical tape, tension bandage or sleeve to secure in place.

Label contents#

Full prescribing information#

Active ingredient (in each patch)

OTC - ACTIVE INGREDIENT SECTION

Menthol 5%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

When using this product: • use only as directed • do not apply to wounds or damaged skin • avoid contact with eyes • do not bandage tightly

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.

If pregnant or breast-feeding  ask a health professional before use.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
  • Children under 2 years of age: Consult a doctor.
  • Clean skin of oil, dirt, lotions, etc. and dry completely before use.
  • If necessary, use medical tape, tension bandage or sleeve to secure in place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

activated charcoal, alcohol, borneol, dihydroxyaluminum aminoacetic acid, disodium EDTA, DMDM ethyl urea, glycerin, polyvinyl pyrrolidone povidone K30, sodium polyacrylate, water

SPL UNCLASSIFIED SECTION

HYDROGEL PATCH with ACTIVATED CHARCOAL

* helps relieve minor aches and pains of muscles and joints

* pain-relieving menthol on a breathable adhesive patch

* hydrogel infused with charcoal for smoother skin

* resealable pouch

* lasts up to 8 hours

VEGAN

No animal products or animal testing

For more info about charcoal and other free health resources, go to lifeandhealth.org

Distributed by Carbon Biotech LLC

110 Flocchini Circle, Ste 400

Lincoln, CA 95648

Made in China

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BlkIce1-2BlkIce1-2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
420222menthol 5 % Medicated PatchPSN1
420222menthol 0.05 MG/MG Medicated PatchSCD1
420222menthol 5 % Medicated PatchSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72411-102-012022-01-28C16284748780-1d6a99b39-4eea-a426-e053-dadaa90af4c2BLACK ICE MEDICATED PATCHES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72411-102-01BLACK ICE MEDICATED PATCHES1 in 1 PACKAGEPATCH11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72411-102BLACK ICE MEDICATED PATCHES (MENTHOL) PATCH [CARBON BIOTECH LLC]1Legacy NDC, 1 package rows20180725_0d16cd14-e6f6-4c47-b151-e1fadd54be35.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
72411-10272411-102-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
c1cc83cd-2cd3-4fc7-bf01-bf0ca293507f0d16cd14-e6f6-4c47-b151-e1fadd54be352018-07-16WarningsExact identifier
spl id: c1cc83cd-2cd3-4fc7-bf01-bf0ca293507f
spl set id: 0d16cd14-e6f6-4c47-b151-e1fadd54be35

Reported adverse events (FAERS/openFDA)#

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