SCRUBIDINE  POVIDONE IODINE SURGICAL SCRUB- 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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Scrubidine Label

Povidone Iodine Surgical Scrub

(0.75% available Iodine)

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

Directions for use: Wet hands with water and pour about 5 ml on the palm of hand.  Scrub thoroughly over all areas in both hands for at least 5 min., using a brush as needed.  Rinse thoroughly under running water.  Repeat as needed.

Directions for use: Wet hands with water and pour about 5 ml on the palm of hand.  Scrub thoroughly over all areas in both hands for at least 5 min., using a brush as needed.  Rinse thoroughly under running water.  Repeat as needed.

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Scrubidine Label

SCRUBIDINE   POVIDONE IODINE SURGICAL SCRUB
povidone iodine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12745-146
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE8.64 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM LAURYL SULFATE (UNII: 368GB5141J) 16.8 g  in 100 mL
LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38) 1.08 g  in 100 mL
SODIUM HYDROXIDE (UNII: 55X04QC32I) 0.311 mL  in 100 mL
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:12745-146-01118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/03/1977
2NDC:12745-146-023785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/03/1977
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C08/03/197709/16/2019
Labeler - Medical Chemical Corporation (008496861)
Establishment
NameAddressID/FEIBusiness Operations
Medical Chemical Corporation008496861manufacture(12745-146)

Revised: 9/2019
Document Id: 92b1c6b4-2fd0-14c0-e053-2a95a90a6372
Set id: 095c47d5-9fe0-45ed-93eb-a2ac3961db59
Version: 11
Effective Time: 20190916
 
Medical Chemical Corporation