FDA.reportPublic FDA data

Wish ultra winter ice

Manufacturer
LJ Pharma
Effective date
2025-08-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:09:11

Label at a glance#

ProductWish ultra winter ice
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure7 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints associated with: Arthritis Simple backache Strains Bruises Sprains Provides cooling relief

Dosage and administration

Clean affected area before applying product Adults and children 2 years and older: Apply to affected area no more than 3 to 4 times daily Children under 2 years of age: Ask a doctor

Label contents#

Full prescribing information#

Active Ingredient                                   Purpose

OTC - ACTIVE INGREDIENT SECTION

Menthol 2%                                          Topical analgesic

Uses

INDICATIONS & USAGE SECTION

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

  • Arthritis
  • Simple backache
  • Strains
  • Bruises
  • Sprains
  • Provides cooling relief

Warnings

WARNINGS SECTION

For external use only

Do not use:

  • With other topical pain relievers
  • With heating pads or heating devices

Stop use and ask a doctor if:

  • Condition worsens
  • Symptoms last more than 7 days and/or subside and occur again within a few days

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 and older: Apply to affected area no more than 3 to 4 times daily
  • Children under 2 years of age: Ask a doctor

Other information

SPL UNCLASSIFIED SECTION

  • store at 20° - 25°C ( 68° - 77° F) [ see USP Controlled Room Temperature], in a tightly closed container
  • store in a cool place 
  • do not use, pour, spill or store near heat or open flame 

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ammonium hydroxide, carbomer, cupric sulfate, FD&C blue no. 1, isopropyl alcohol, magnesium sulfate, purified water, sodium hydroxide, thymol

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311502menthol 2 % Topical GelPSN1
311502menthol 0.02 MG/MG Topical GelSCD1
311502menthol 2 % Topical GelSY1
311502menthol 2 % topical stickSY1

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84809-008-01Wish ultra winter ice200 g in 1 BOTTLEGEL2001

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84809-00884809-008-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMMONIA5138Q19F1XIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
CUPRIC SULFATELRX7AJ16DTIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
ISOPROPYL ALCOHOLND2M416302IACT
MAGNESIUM SULFATE, UNSPECIFIED FORMDE08037SABIACT
WATER059QF0KO0RIACT
SODIUM HYDROXIDE55X04QC32IIACT
THYMOL3J50XA376EIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB

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
Wish ultra winter iceMENTHOLLJ Pharmab4c5487c-1314-4d63-96df-077e72e7ee952025-08-01WarningsExact identifier
ndc (package): 84809-008-01
ndc (product): 84809-008
ndc11 (package): 84809000801
spl id: 3b4d3df6-aa44-e03a-e063-6294a90a1b9c
spl set id: b4c5487c-1314-4d63-96df-077e72e7ee95

Reported adverse events (FAERS/openFDA)#

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