ZEE POVIDONE IODINE (povidone iodine 10% w/w- equivalent to iodine 1% swab

Zee Povidone Iodine by

Drug Labeling and Warnings

Zee Povidone Iodine by is a Otc medication manufactured, distributed, or labeled by Cintas Corporation, James Alexander Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients (each swab)

10% Povidone Iodine Solution USP, (1% available Iodine)

PURPOSE

Purpose

​​Topical Antiseptic

INDICATIONS & USAGE

Uses

To treat minor skin cuts, and abrasions.

Warnings

FOR EXTERNAL USE ONLY

ASK DOCTOR

Ask a doctor before use if you have

• deep or puncture wounds
• serious burns

STOP USE

Stop use and ask a doctor if

• redness, irritation, swelling or pain persists or increases
• infection occurs

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions:

Reverse cardboard sleeve then crush at dot between thumb and forefinger. Allow
solution to saturate tip and apply solution to injury. 

STORAGE AND HANDLING

Other Information

Store at room temperature away from light keep from freezing or excessive heat.

INACTIVE INGREDIENT

Inactive Ingredients

Citric acid, disodium phosphate, nonoxynol-9, sodium hydroxide, water.​

QUESTIONS

Questions?
Call 1-908-362-9266 Monday through Friday, 9:00 am - 5:00 pm e.s.t.

Package Principal Display Panel

10 SWABS

(1/2 ml.)

UNIT NO.

U1-16A

POVIDONE - IODINE SWABS U.S.P

(ANTISEPTIC)

CONTAINS: POVIDONE IODINE 10%

EQUIVALENT TO 1% AVAILABLE IODINE

ZEE®

Distributed by: ZEE Medical Distributors, LLC

Mason, OH 45040

INGREDIENTS AND APPEARANCE

ZEE POVIDONE IODINE 
povidone iodine 10% w/w (equivalent to iodine 1%) swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42961-023
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
NONOXYNOL-9 (UNII: 48Q180SH9T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42961-023-01	10 in 1 BOX	05/12/2022
1		0.5 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	05/12/2022

Labeler - Cintas Corporation (056481716)

Establishment
Name	Address	ID/FEI	Business Operations
James Alexander Corporation		040756421	manufacture(42961-023)