POVIDONE-IODINE PREP PAD - povidone-iodine swab 
Yinjing Medical Technology (Shanghai) Co., Ltd.

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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POVIDONE-IODINE PREP PAD

Drug Facts


Active Ingredients

Povidone-Iodine 10% w/w
(1% titratable iodine)

Purpose

Antiseptic

Use

First aid antiseptic to help prevent infection in scrapes, minor cuts and burns Antiseptic to prepare skin prior to surgery. Uses antiseptic skin preparation

Stop Use Section

Stop use and ask a doctor if skin irritation, redness, swelling, or pain occurs.

Warnings Section

Warnings • Do not use if allergic to iodine • For external use only • Do not use in eyes • Avoid pooling beneath patient • In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

Keep Out of Reach of Children Section

Keep out of reach of children.

Directions Section

Directions apply locally as needed

Inactive Ingredients Section

Inactive ingredients Sodium hydroxide, water

Other Information Section

Other information
For Hospital or Professional Use Only.
Store at room temperature: 15℃- 30 ℃

Shanghai Yinjing Medical Supplies Co., Ltd.
No.586 Yuanxi RD.Nanhui Industry Park,Shanghai 201300
Tel:+86-21-68016633  Http://www.yinjing.cn
Made in China
LOT                           EXP.

inin
NDC:44019-211-01
1 pad/pouch

POVIDONE-IODINE PREP PAD

For External Use Only

Product Label

povidone-iodine prep pad

POVIDONE-IODINE PREP PAD  
povidone-iodine swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44019-211
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE10 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:44019-211-011 in 1 POUCH08/03/2016
10.45 g in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/03/2016
Labeler - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)
Registrant - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)

Revised: 12/2017
Document Id: 615940bc-14e9-3e74-e053-2a91aa0a22ae
Set id: 149eb720-789b-4706-8d64-e26199d7d541
Version: 5
Effective Time: 20171227
 
Yinjing Medical Technology (Shanghai) Co., Ltd.