WISH ULTRA WINTER ICE- menthol gel

Wish ultra winter ice by

Drug Labeling and Warnings

Wish ultra winter ice by is a Otc medication manufactured, distributed, or labeled by LJ Pharma. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient                                   Purpose

Menthol 2%                                          Topical analgesic

PURPOSE

Uses

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

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

Warnings

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.

KEEP OUT OF REACH OF CHILDREN

Directions

• 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

• 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

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

Questions or Comments? 1-888-402-0184

Product label

INGREDIENTS AND APPEARANCE

WISH ULTRA WINTER ICE 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84809-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
AMMONIA (UNII: 5138Q19F1X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CUPRIC SULFATE (UNII: LRX7AJ16DT)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
THYMOL (UNII: 3J50XA376E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84809-008-01	200 g in 1 BOTTLE; Type 0: Not a Combination Product	07/25/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/25/2025

Labeler - LJ Pharma (914078633)

Establishment
Name	Address	ID/FEI	Business Operations
LJ Pharma		914078633	manufacture(84809-008)