Iodine Sepp description, usages, side effects, indications, overdosage, supplying and lots more!

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Iodine Sepp

CareFusion 213 LLC
CareFusion 2200, Inc

Iodine Tincture 2%


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Iodine 2% v/v, USP

Purpose

Antiseptic

Use

  •  patient preoperative skin preparation. Helps to reduce bacteria that potentially can cause skin infection.

Warnings

For external use only. Flammable: Keep away from fire or flame.

Do not use with electrocautery procedures

Do Not Use

  • •in the eyes
  • •on patients with known allergies to ethyl alcohol or iodine

When using this product

keep out of eyes, ears, and mouth

Stop use and ask a doctor if

irritation, sensitization, or allergic reaction occurs. You may report side effects to FDA at 1-800-FDA-1088.

Keep out of reach of children.

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

Directions

  • 1remove the applicator wrapper. Do not touch the applicator tip.
  • 2with the applicator tip facing downward, pinch the barrel of the applicator ONCE to release the antiseptic.
  • 3Press the applicator tip against the patient’s skin. With gentle back and forth actions apply solution to the treatment area.
  • 4the area covered should be allowed to dry naturally.
  • 5discard after a single use.

Iodine Sepp Other information

  •  store below 30 °C (86 °F)

Inactive ingredients

  •  Ethyl alcohol, USP purified water, sodium iodide USP

Questions?

call 1-800-523-0502 (M-F 8 a.m.-5 p.m. CST)

Package/Label Principal Display Panel

Cat. No. 260261

NDC 54365-161-01

Single Use

Not made with natural rubber latex.

Applicator is sterile if package is intact.

200 Applicators

0.02 fl. oz. (0.67ml) each

Iodine Sepp

Iodine TINCTURE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:54365-161
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Iodine IODINE 20 mg

Inactive Ingredients

Ingredient Name Strength
sodium iodide
ALCOHOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 0.67 in 1 APPLICATOR
2 1 in 1 POUCH
3 NDC:54365-161-01 200 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 1988-02-01


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Be sure to consult your doctor before taking any medication!
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