POVIDONE-IODINE description, usages, side effects, indications, overdosage, supplying and lots more!

POVIDONE-IODINE

LernaPharm Loris 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
DRUG FACTS

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients (in each Swab)


Povidone Iodine 10% w/v

Purpose

Antiseptic

Uses



Warnings

For External Use only

OTC -Do Not Use Section

Do not use in the eyes ● Apply over a large areas of the body ● In case of deep puncture wounds, animal
bites, or serious burns, consult a doctor.

OTC -Stop Use Section

Stop use and consult a doctor if the condition persists or gets worse.

Other Required Warnings

Do not use longer than 1 week unless directed by the doctor.

Directions

● 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 ● If bandaged, let dry first.

Other Information

Store at room temperature between 59 - 86 0F (15 - 30 0C)

Inactive Ingredients



Principal Display Panel

NDC: 68356-109-01                                                PRODUCT # 109-01U

LORIS 10% PVP - I SOLUTION

MEDIUM

200 Antiseptic swabs saturated with 10% W/V Povidone Iodine solution, USP

(equivalent to 1% available iodine)

200                                                  For external Use OnlyPrincipal Display Panel

POVIDONE-IODINE

POVIDONE-IODINE SWAB

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68356-109
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
POVIDONE-IODINE IODINE 0.05 g

Inactive Ingredients

Ingredient Name Strength
water
SODIUM HYDROXIDE
COPOVIDONE
GLYCERIN
SODIUM LAURYL SULFATE
PHOSPHORUS
SODIUM CITRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68356-109-01 200 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part333 2010-01-04


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Be sure to consult your doctor before taking any medication!
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