EVERLIT SURVIVAL IODINE PREP PADS- povidone-iodine prep pads cloth 
EVERLIT GLOBAL INC.

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Everlit Survival Iodine Prep Pad

Active Ingredient

Povidone Iodine 10%

Purpose

Antiseptic

Uses

Antiseptic cleanser to help prevent skin infection in minor cuts, scrapes, and burns

For preparation of the skin prior to surgery

Helps reduce bacteria that can potentially cause skin infection

Warnings

For External Use Only.

Do not use

In the eyes

As a first aid anticeptic for more than 1 week

Over large areas of the body

Ask a doctor before use if you have

Deep puncture wounds

Animal bites

Serious wounds

Stop use and ask a doctor if

Condition worsens or persists for more than 72 hours

Irritation and redness develops

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately

Directions

Tear a notch

Remove applicator

Use only once

As a first aid antiseptic

Clean affected area

apply 1 to 3 times daily

May be covered with sterile bandage

If bandaged, let dry first

For preoperative patient skin preparation

Clean area

Apply to operative site prior to surgery using applicator

Other Information

Store at room temperature

Avoid excessive heat

Inactive Ingredients

Nonoxynol-9, water

DOSAGE & ADMINISTRATION

Sterile unless poch is opened or damaged.

Saturated with 10% Povidone Iodine.

INDICATIONS & USAGE

For External Use Only. Apply topically as needed. Discard after single use.

Everlit Survival Iodine Prep Pad

Iodine Prep Pad

EVERLIT SURVIVAL IODINE PREP PADS 
povidone-iodine prep pads cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83807-018
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE0.54 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
NONOXYNOL-9 (UNII: 48Q180SH9T)  
Product Characteristics
ColorbrownScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83807-018-011 in 1 BAG; Type 0: Not a Combination Product12/26/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00312/26/2023
Labeler - EVERLIT GLOBAL INC. (122311450)
Registrant - EVERLIT GLOBAL INC. (122311450)
Establishment
NameAddressID/FEIBusiness Operations
Yangzhou Suxiang Medical Instrument Co, LTD543387280manufacture(83807-018)

Revised: 12/2023
Document Id: 0d4d8991-d2c7-4bdd-e063-6294a90ae913
Set id: 0d4d8f5a-db1e-60e0-e063-6294a90aae77
Version: 1
Effective Time: 20231226
 
EVERLIT GLOBAL INC.