WHITE FLOWER ANALGESIC BALM description, usages, side effects, indications, overdosage, supplying and lots more!

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WHITE FLOWER ANALGESIC BALM

JELMA PHILIPPINES INC

DRUG FACTS




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients
Camphor 6%
Menthol 15%
Methyl salicylate 40%

Purpose

Purpose
External analgesic


Uses
  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

Do not use

  • on wounds
  • on irritated or damaged skin
  • on the face
  • otherwise than as directed

When using this product

  • avoid contact with the eyes or mucous membranes
  • do not bandage tightly

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days
  • excessive irritation of the skin develops
  • nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs
  • when using for pain of arthritis
    • pain persists for more than 10 days
    • redness is present
    • in conditions affecting children under 12 years of age

Keep out of reach of children to avoid accidental poisoning.
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults and children 3 years of age and older: Apply a few drops then gently rub into the affected area not more than 3 to 4 times daily.
  • Children under 3 years of age: Do not use, consult your doctor.
  • Refer to the above warnings; use otherwise than as directed may be dangerous.

Other information

  • keep container tightly closed
  • store at 15º to 30ºC (59º to 86ºF)

Inactive ingredients
Eucalyptus oil, lavender oil and peppermint oil.

Questions or comments? (888)221-3496 M-F 9am to 5pm

  • you may also report serious side effects to this phone number

WHITE FLOWER ANALGESIC BALM  NDC-51681-0001-1  0.67 fl oz (20mL)WHITE FLOWER ANALGESIC BALM

WHITE FLOWER ANALGESIC BALM

CAMPHOR, MENTHOL, AND METHYL SALICYLATE OIL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51681-0001
Route of Administration TRANSDERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CAMPHOR (SYNTHETIC) 6 g
MENTHOL 14.6 g
methyl salicylate METHYL SALICYLATE 40 g

Inactive Ingredients

Ingredient Name Strength
EUCALYPTUS OIL
LAVENDER OIL
PEPPERMINT OIL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51681-0001-1 20 in 1 BOTTLE, GLASS
2 NDC:51681-0001-2 10 in 1 BOTTLE, GLASS
3 NDC:51681-0001-4 2.5 in 1 BOTTLE, GLASS
4 NDC:51681-0001-3 5 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2010-06-14


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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