ICEQUAKE ANALGESTIC WHITE- methyl salicylate, menthol cream

IceQuake Analgestic White by

Drug Labeling and Warnings

IceQuake Analgestic White by is a Otc medication manufactured, distributed, or labeled by Southern Sales & Service, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Menthyl Salicylate 10%

Menthol 2%

Purpose

Topical Analgesic

Topical Analgesic

Uses

For temporary relief of minor aches and pains of muscles and joints associated with

• Arthritis
• Simple backache
• Strains
• Sprains
• Bruises

Warnings

For external use only

Discontinue use if excessive irritation of the skin develops. Caution: 

• avoid contact with eyes and mucous membranes
• do not use otherwise than as directed

When using this products

• do not bandage tightly
• do not apply to wounds or damaged skin.

Stop use and ask a doctor if

• condition worsens
• 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.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions

apply to affected area not more than 3 to 4 times daily. Audlts and children 12 years of age and older:

: consult a doctor. Children under 12 years of age

Other Information

store at room temperature 15° - 30°C (59° - 86°F)

close cap tightly after use.

Inactive Ingredients

mineral oil, propylene gylcol, cetyl stearyl alcohol, purified water, ceteareth-6, stearyl alcohol, PEG-20 cetyl/stearyl ether, methylparaben, propylparaben.

IceQuake Topical Analgestic Cream White 60g

INGREDIENTS AND APPEARANCE

ICEQUAKE ANALGESTIC WHITE 
methyl salicylate, menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69822-310
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	10 g  in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
WATER (UNII: 059QF0KO0R)
CETEARETH-6 (UNII: 2RJS3559D3)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69822-310-02	60 g in 1 TUBE; Type 0: Not a Combination Product	08/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	08/01/2022

Labeler - Southern Sales & Service, Inc. (013114906)

Registrant - Southern Sales & Service, Inc. (013114906)