Tincture Merthiolate description, usages, side effects, indications, overdosage, supplying and lots more!

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Tincture Merthiolate

DLC Laboratories, Inc

Tincture Merthiolate


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

First Aid Antiseptic

Tincture Merthiolate Uses

first aid to help prevent infection in minor:
cuts - scrapes - burns - insect bites

Warnings

For external use only.
Consult a doctor before use if you have - deep or puncture wounds - animal bites - serious burns

When using this product

  • do not use in or near the eyes
  • do not apply in large quantities or over large areas of the body
  • do not apply over raw surtaces or blistered areas

Stop use and consult a doctor if

  • redness, irritation, swelling or pain persists or increases, or il infection or rash occurs
  • symptoms persist for more than 7 days, or clear up and occur again within a lew days

Keep out of reach of children.

II swallowed, get medical help or contact a Poison Control Center immediately.

Directions

  • adults and children 2 years of age and older: clean the affected area
  • apply a small amount of this product to the area using the enclosed applicator or a cotton-tipped applicator 1 to 3 times daily _ may be covered with a sterile bandage (let dry first)
  • children under 2 years, ask a doctor

Other Information

  • medication will stain skin and clothing

Inactive Ingredients

acetone, alcohol, DandC red no. 22, purified water

Product Labeling

De La Cruz

Tincture Merthiolate

50% Alcohol

Mercury Free

For external use only

First Aid Antiseptic

1 FL OZ

Manufactured by
De La Cruz Products
A Division of DLC Laboratories, Inc.
Paramount, CA 90723 USA
Questions: 1-800-858-3889
www.dlclabs.com

Warnings: do not use if plastic seal around cap is broken or removed. For external use only.

Tincture Merthiolate

Tincture Merthiolate

BENZALKONIUM CHLORIDE TINCTURE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:24286-1532
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 1.3 mg

Inactive Ingredients

Ingredient Name Strength
acetone
ALCOHOL
D&C RED NO. 22
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:24286-1532-7 30 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2013-03-22


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