DECOLORIZED IODINE- ethyl alcohol liquid 
Pharma Nobis, LLC

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Private Label Decolorized Iodine

Drug Facts

Active Ingredients

Alcohol 45 % denatured with ammonia, Ammonium and Potassium Iodides.

Purpose

Antiseptic

Uses

First aid to help prevent infection in minor cuts, scrapes and burns.

Warnings

For external use only.

Ask a doctor before use if you have

deep or puncture wounds, animal bites, serious burns.

Stop use and ask a doctor if:

The condition persists or gets worse, or if using this product for longer than 1 week.

When using this product:

Do not use in the eyes. If contact occurs, flush with large amounts of water while lifting upper and lower lids. Do not apply over large areas of the body.

Keep out of the reach of children.

In case of acidental ingestion give milk, then give a starch solution made by mixing two tablespoonfools of cornstarch or flour to a pint of water. contact a poison Control Center immediately.

Directions

Clean the affected area. Aply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let it dry first.

Inactive Ingredient:

Purified Water

Other Information:

Will stain skin and clothing

De La Cruz Label

DLC

Good Neighbor Label

GNP

Leader Label

Leader

Quality Choice Label

QC

Sunmark Label

SM

DDM Label

DDM

Rite Aid Label

RA

CVS Label

CVS Decolorized 2022CVC

Top Care Label

TC

Vida Mia Label

VM

Health Mart Label

HM

DECOLORIZED IODINE 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82645-909
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.45 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
AMMONIA (UNII: 5138Q19F1X)  
IODINE (UNII: 9679TC07X4)  
POTASSIUM IODIDE (UNII: 1C4QK22F9J)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82645-909-9259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/23/2022
2NDC:82645-909-9130 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/23/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00306/23/2022
Labeler - Pharma Nobis, LLC (118564114)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114manufacture(82645-909) , analysis(82645-909) , pack(82645-909) , label(82645-909)

Revised: 12/2023
Document Id: 0d1ce3b4-41f8-98a4-e063-6394a90a7eaf
Set id: e21dd43b-3712-cb16-e053-2a95a90ac276
Version: 2
Effective Time: 20231222
 
Pharma Nobis, LLC