De La Cruz Mercurochrome description, usages, side effects, indications, overdosage, supplying and lots more!

De La Cruz Mercurochrome

DLC Laboratories, Inc.
DLC Laboratories, Inc.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Mercurochrome

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Benzalkonium Chloride 0.13%

Liddocaine Hydrochloride 2.5%

Purpose

First Aid Antiseptic

Pain Reliever

Uses

first aid to help prevent bacterial contamination or skin infection and temporarily relieves pain and itching associated with cuts, scrapes, burns, sunburn, skin irritations

Warnings

For external use only.

Ask a dotor 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 over large ares of the body or in large quantities. do not apply over raw surfaces or blistered areas.

Stop use and ask a doctor if

condition worsens, symptoms persist for more than 7 days, or clear up and occur again with in a few days.

Keep out of the 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: clean the affected area; apply a small amount of this product on the area 1 to 3 times daily; may be covered with a sterile bandage (let dry first). children unde4r 2 years, ask a doctor

Other Information

protect from excessive heat


Inactive Ingredients

acetone, purified water USP

De La Cruz

Mercurochrome

(Benzalkonium Chloride and Lidocaine hydrochloride)














De La Cruz Mercurochrome

BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:24286-1553
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.13 mL
LIDOCAINE HYDROCHLORIDE LIDOCAINE 2.5 mL

Inactive Ingredients

Ingredient Name Strength
acetone
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:24286-1553-1 30 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2011-06-30


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