Ice Cold Analgesic Gel description, usages, side effects, indications, overdosage, supplying and lots more!

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Ice Cold Analgesic Gel

Universal Distribution Center LLC
Anicare Pharmaceuticals Pvt. Ltd




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients

Menthol             1.0%

Camphor            0.5%

Purpose

Purpose

Topical Analgesic

Uses

Uses

for the temporary relief  of minor aches and pains in muscles and joints associated with:

  • simple backache
  • strains
  • sprains
  • sports injuries
  • arthritis
  • bruises

Warnings

For external use only

Do not use

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

When using this product

  • do not use in or near eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

Stop use and ask doctor if

  • condition worsens
  • symptoms last more than 7 days or clean up and occur again within a few days
  • redness or irritation develops

If pregnant or breast-feeding, ask a health professional before use

Keep out of the reach of children

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

Directions

  • clean affected area before applying product
  • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily

Inactive ingredients

benzyl alcohol, butylated hydroxytoluene, carbopol, colour brillient blue, creasmer RH 40, disodium EDTA, isopropyl alcohol, propylene glycol, purified water and sodium hydroxide

PRINCIPAL DISPLAY PANEL

ICE COLD ANALGESIC GEL

Topical Analgesic
NET WT.8 OZ (227g)

Ice Cold Analgesic Gel



Ice Cold Analgesic Gel

Menthol and Camphor GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52000-013
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 1 g
CAMPHOR (SYNTHETIC) 0.5 g

Inactive Ingredients

Ingredient Name Strength
BENZYL ALCOHOL
BUTYLATED HYDROXYTOLUENE
CARBOMER 934
FD&C BLUE NO. 1
EDETATE DISODIUM
ISOPROPYL ALCOHOL
propylene glycol
SODIUM HYDROXIDE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52000-013-17 127 in 1 TUBE
2 NDC:52000-013-18 170 in 1 TUBE
3 NDC:52000-013-13 170 in 1 BOTTLE, PLASTIC
4 NDC:52000-013-14 227 in 1 BOTTLE, PLASTIC
5 NDC:52000-013-15 300 in 1 BOTTLE, PLASTIC
6 NDC:52000-013-16 500 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2013-03-15


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Be sure to consult your doctor before taking any medication!
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