FDA.reportPublic FDA data

Walgreens Ice Blue Gel

Manufacturer
Walgreens Company | ANICARE PHARMACEUTICALS PRIVATE LIMITED
Effective date
2024-12-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:44:59

Label at a glance#

ProductWalgreens Ice Blue Gel
Active ingredientMENTHOL
Label structure12 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints associated with simple backache arthritis strains bruises sprains

Dosage and administration

Clean affected area before applying product Adults and children 2 years and older, apply to the affected area not more than 3 to 4 times daily Children under 2 years of age, ask a doctor before using this product

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 2%

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

  • Do not use with other topical pain relievers
  • Do not use with heating pads or other heating devices
  • Avoid contact with eyes
  • Do not bandage tightly
  • Do not apply to wounds or damage skin

Stop use and ask a doctor if:

OTC - STOP USE SECTION

Condition worsens, or if symptoms persist for more than 7 day or clear up and occur again withing a few days

If pregnant or breastfeeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact Poison Control Center (800-222-1222) right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean affected area before applying product
  • Adults and children 2 years and older, apply to the affected area not more than 3 to 4 times daily
  • Children under 2 years of age, ask a doctor before using this product

Other Information

OTHER SAFETY INFORMATION

  • Do not freeze
  • Store at room temperatiure
  • Keep container tightly closed when not in use
  • do not use, pour, spill or store near heat or open flame

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ammonium hydroxide, benzyl alcohol, carbopol 940, cupric sulphate, FD&C blue no.1, isopropyl alcohol, magnesium sulphate, PEG-40, hydrogenated castor oil, sodium hydroxide, thymol, water

Walgreens Ice Blue Gel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311502menthol 2 % Topical GelPSN3
311502menthol 0.02 MG/MG Topical GelSCD3
311502menthol 2 % Topical GelSY3
311502menthol 2 % topical stickSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-9621-012025-07-29C16284748780-13b156c62-2c9a-fb37-e063-e6dba90a4e07Walgreens Ice Blue Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-9621-01Walgreens Ice Blue Gel226.8 g in 1 JARGEL226.83

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-9621WALGREENS ICE BLUE GEL (MENTHOL) GEL [WALGREENS COMPANY]3Legacy NDC, 1 package rows20241220_cf5966f8-bd0b-2942-e053-2995a90a5cab.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
0363-96210363-9621-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
THYMOL3J50XA376EIACT
CARBOMER 9404Q93RCW27EIACT
BENZYL ALCOHOLLKG8494WBHIACT
CUPRIC SULFATELRX7AJ16DTIACT
MAGNESIUM SULFATE, UNSPECIFIEDDE08037SABIACT
MENTHOLL7T10EIP3AACTIB
WATER059QF0KO0RIACT
AMMONIA5138Q19F1XIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
ISOPROPYL ALCOHOLND2M416302IACT
SODIUM HYDROXIDE55X04QC32IIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

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
2981cb97-17e3-ebda-e063-6394a90ad281cf5966f8-bd0b-2942-e053-2995a90a5cab2024-12-17WarningsExact identifier
spl id: 2981cb97-17e3-ebda-e063-6394a90ad281
spl set id: cf5966f8-bd0b-2942-e053-2995a90a5cab

Reported adverse events (FAERS/openFDA)#

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