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Medicated

Vi-Jon
Vi-Jon

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Menthol 0.15%

Zinc oxide 1.0%

Purpose

External analgesic

Skin protectant

Medicated Uses

Uses for the temporary relief of paina and itching due to:

  • monor cuts
  • sunburn
  • insect bites
  • poison ivy
  • poison oak
  • poison sumac
  • scrapes
  • minor burns
  • minor skin irritations

dries the oozing and weeping of:

  • poison ivy
  • poison oak
  • poison sumac

Warnings

For external use only

When using this product

avoid contact with the eyes

Stop use and ask a doctor if

condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children

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

Directions

adults and children 2 years of age and older - apply to affected area not more than 3 to 4 times daily

children under 2 years of age - do not use, consult a doctor

  • for best results dry skin thoroughly before applying

Inactive ingredients

 talc, acacia, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate

disclaimer

This product is sold by weight, not by volume. Some settling may occur during handling and shipping

Made in the USA with US and foreign components

Side Effects

Vi-Jon

One Swan Drive

Smyrna, TN 37167

Principal Display Panel

NDC 0869-0551-38

SWAN

medicated

Body Powder

skin protectant/topical analgesic

triple action

  • Cooling
  • Absorbing
  • Itch Relieving

Compare to Active Ingredients of Gold Bond Medicated Body Powder

NET WT 10 OZ (283 G)

Medicated

Medicated

menthol, zinc oxide POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0869-0551
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 1.5 mg
Zinc Oxide Zinc oxide 10 mg

Inactive Ingredients

Ingredient Name Strength
talc
ACACIA
EUCALYPTOL
methyl salicylate
Salicylic Acid
THYMOL
ZINC STEARATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0869-0551-38 283 in 1 BOTTLE, DISPENSING

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2003-08-12


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