Lander Polar Ice

Dosage form: gel
Ingredients: Menthol 20mg in 1g
Labeler: Abaco Partners LLC DBA Surefil
NDC code: 20890-0020

Medically reviewed by Drugs.com. Last updated on Oct 9, 2023.

LANDER®
POLAR ICE
TOPICAL ANALGESIC GEL

Drug Facts

Active Ingredients

Menthol, 2.0%

Purpose

Topical analgesic

Uses

Temporarily relieves:

-: Minor muscle aches and pains

Warnings

For external use only; avoid contact with eyes

When using this product, do not;

-: heat
-: microwave
-: add to hot water or any container where heating water may cause splattering and result in burns
-: use in eyes or directly on mucous membranes
: take by mouth or place in nostrils
-: apply to wounds or damaged skin
-: bandage skin

Consult a doctor and discontinue use:

If condition worsens, persists for more than 1 week or tends to recur.

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center Immediately.

Directions

For the temporary relief of minor muscle aches and pains. See important warnings under "When using this products"

-: not for use on children under 2 years of age
-: adults & children 2 years & older: apply liberally to painful area and massage until gel is absorbed into the skin. Repeat 3 to 4 times daily.

Inactive Ingredients

FD&C Blue #1, Camphor, Carbomer, Isopropyl Alcohol, Methylchloroisothiazolinone, Methylisothiazolinone, Nonoxynol - 9, Propylene Glycol, Sodium Hydroxide, Water.

Polar Ice® is a registered trademark of Grand Brands LLC, Grand
Rapids, MI 49512 USA

UPC: 8-14344-0-1123-9

PRINCIPAL DISPLAY PANEL - 226g Container

LANDER®
America's Health & Beauty Care Company

POLAR
ICE
TOPICAL ANALGESIC GEL

NET WT. 8 OZ (226g)

Made in U.S.A.

LANDER POLAR ICE
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:20890-0020
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Menthol (Menthol)	Menthol	20 mg in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water
Propylene Glycol
Camphor (SYNTHETIC)
Nonoxynol-9
Isopropyl Alcohol
Carbomer Homopolymer Type C
Sodium Hydroxide
FD&C Blue NO. 1
Methylchloroisothiazolinone
Methylisothiazolinone

Product Characteristics
Color	BLUE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description
1	NDC:20890-0020-1	226 g in 1 CONTAINER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part356	12/01/2010

Labeler - Abaco Partners LLC DBA Surefil (964809417)

Establishment
Name	Address	ID/FEI	Operations
Anicare Pharmaceutical Pvt.		916837425	MANUFACTURE

Document Id: 6cc082b1-ae18-49ed-a51b-d1c5c28792ee

Set id: 35abbfe2-39a3-4f24-b23e-84d8614e07e7

Version: 1

Effective Time: 20101018

Abaco Partners LLC DBA Surefil

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer