Lucky Ice Cold Analgesic

Manufacturer
Delta Brands Inc
Effective date
2023-09-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:26:21

Label at a glance#

ProductLucky Ice Cold Analgesic
Active ingredientMENTHOL
Label structure12 sections

Indications and uses

temporary relieves minor aches and pains of muscles and joints associated with: ■ arthritis ■ simple backache ■ strains ■ bruises ■ sports injuries ■ sprains ■ provides cooling penetrating relief

Dosage and administration

■ clean affected area before applying product. ■ adults and children 2 years of age and older: apply to affected area not more than 3-4 times daily ■ children under 2 years of age: ask a doctor

Storage and handling

■ store at controlled room temperature 20 to 25ºC (68 to 77ºF) in a tightly closed container ■ do not use, pour, spill or store near heat or open flame

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.25%

Purpose

OTC - PURPOSE SECTION


Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

temporary relieves minor aches and pains of muscles and joints associated with:

■ arthritis ■ simple backache ■ strains ■ bruises ■ sports injuries ■ sprains ■ provides cooling penetrating relief

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

■ with other topical pain relievers ■ with heating pads or heating devices

When using this product

OTC - WHEN USING SECTION

■ do not use in or near the eyes ■ do not apply to wounds or damaged skin ■ do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ condition worsens ■ symptoms last more than 7 days or clear up and occur again within a few days ■ redness or irritation develops

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ clean affected area before applying product. ■ adults and children 2 years of age and older: apply to affected area not more than 3-4 times daily ■ children under 2 years of age: ask a doctor

Other information

STORAGE AND HANDLING SECTION

■ store at controlled room temperature 20 to 25ºC (68 to 77ºF) in a tightly closed container ■ do not use, pour, spill or store near heat or open flame

Inactive Ingredients

INACTIVE INGREDIENT SECTION

benzyl alcohol, BHT, camphor, carbopol, disodium EDTA, FD&C blue no.1, isopropyl alcohol, PEG-40 hydrogenated castor oil, propylene glycol, sodium hydroxide, water

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
20276-21120276-211-07, 20276-211-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
04cad5ea-ec4e-d17a-e063-6294a90a68f5ddce5f6e-599a-7148-e053-2a95a90a9a482023-09-07WarningsExact identifier
spl id: 04cad5ea-ec4e-d17a-e063-6294a90a68f5
spl set id: ddce5f6e-599a-7148-e053-2a95a90a9a48

Reported adverse events (FAERS/openFDA)#

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