Surgicide Label

Drug Labeling and Warnings

Drug Details [pdf]

SURGICIDE  POVIDONE IODINE- povidone iodine liquid 
Medical Chemical Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Surgicide Label

Surgicide is a broad spectrum topical antiseptic for use on skin and mucous membranes.  Use solution without dilution as needed.

10% Povidone Iodine Solution, USP

Warning: Contains Iodine.  In case of accidental ingestion call a physician or poison control center and treat for Iodine poisoning.  Keep out of the the reach of children.

Warning: Contains Iodine.  In case of accidental ingestion call a physician or poison control center and treat for Iodine poisoning.  Keep out of the the reach of children.

Directions: apply Surgicide without dilution, as often as needed.  In case of deep or puncture wounds consult a physician.  If redness, swelling, or irritation persists, call a physician.

Directions: apply Surgicide without dilution, as often as needed.  In case of deep or puncture wounds consult a physician.  If redness, swelling, or irritation persists, call a physician.

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surgicidelabel.jpg

SURGICIDE   POVIDONE IODINE
povidone iodine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12745-144
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	10.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 12745-144-01	1 mL in 1 VIAL; Type 0: Not a Combination Product	08/03/1977
2	NDC: 12745-144-02	20 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/03/1977
3	NDC: 12745-144-03	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/03/1977
4	NDC: 12745-144-04	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/03/1977
5	NDC: 12745-144-05	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/03/1977
6	NDC: 12745-144-06	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/03/1977

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	08/03/1977	09/16/2019

Labeler - Medical Chemical Corporation (008496861)

Establishment
Name	Address	ID/FEI	Business Operations
Medical Chemical Corporation		008496861	manufacture(12745-144)

Revised: 9/2019

Document Id: 92b1b7ae-7cc6-dd4d-e053-2a95a90a37ce

34390-5

Set id: 74a2cbd9-a16f-4819-a45d-3efc2f23c071

Version: 12

Effective Time: 20190916