Perfect Purity HotIce description, usages, side effects, indications, overdosage, supplying and lots more!

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Perfect Purity HotIce

Davion, Inc dba HABA
Anicare Pharmaceuticals Pvt. Ltd

Perfect Purity HotIce Gel




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient

Menthol 1%                                

Purpose

Purpose

Topical Analgesic

Uses

Uses

Provides temporary relief of minor aches and pains in muscles and joints associated with simple backache, strains, sprains, arthritis and sports injuries.

Warnings

For external use only. Not for internal use.

Use only as directed. Avoid contact with eyes or mucous membranes.  Do not apply to open wounds or damaged skin. Make sure skin is clean and free from any creams, ointments, sprays or liniment. Do not bandage.

Do not use with heating pads or heating devices.

If condition worsens, symptoms persist for more than 7 days or if symptoms disappear and occur again within a few days, discontinue use and consult a physician.  If you are pregnant or nursing a baby, consult your doctor before use

Do not use, store, pour, spill near heat or open flame.

Store in a cool, dry place and keep lid tightly closed.

Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center immediately.

Directions

Clean skin of all other lotions, creams, ointments, liniments or sprays.

Apply liberally to affected area and massage until gel is absorbed into the skin.

Do not apply more than 3 or 4 times daily. No protective cover needed. Do not apply to children under 2 years of age.

Inactive Ingredients

Water, Isopropyl Alcohol, Nonoxylon-10,  Camphor, Carbomer, Sodium Hydroxide, Methylchloroisothiazolinone, Methylisothiazolinone and Blue 1 (CI 42090).

Perfect Purity HotIce Gel

Topical Analgesic

Net Wt. 8 OZ (227g)

Perfect Purity HotIce

Perfect Purity HotIce

Menthol GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42669-998
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 1.0 g

Inactive Ingredients

Ingredient Name Strength
water
ISOPROPYL ALCOHOL
NONOXYNOL-10
CAMPHOR (SYNTHETIC)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)
SODIUM HYDROXIDE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42669-998-02 227 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2013-12-24


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Be sure to consult your doctor before taking any medication!
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