FDA.reportPublic FDA data

Quality Choice Iodides Tincture

Manufacturer
Chain Drug Market Association | Pharma Nobis, LLC
Effective date
2023-12-20
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:05:09

Label at a glance#

ProductQuality Choice Iodides Tincture
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

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

Dosage and administration

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.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

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

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

deep or puncture wounds, animal bites, serious burns.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

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

When using this product:

OTC - WHEN USING SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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:

INACTIVE INGREDIENT SECTION

Purified Water

Other Information:

OTHER SAFETY INFORMATION

Will stain skin and clothing. FLAMMABLE: Keep away from spark, heat & flame.

Principal Package Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

QCDecolorized.jpgQCDecolorized.jpgLabel 60 mlLabel 60 ml

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63868-331-02Quality Choice Iodides Tincture60 mL in 1 BOTTLE, PLASTICLIQUID606

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63868-331QUALITY CHOICE IODIDES TINCTURE (ETHYL ALCOHOL) LIQUID [CHAIN DRUG MARKET ASSOCIATION]6Current NDC, Legacy NDC, 1 package rows20231221_71aedfd5-e81f-4b69-b163-527ff1ce30b1.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63868-331-02ML - Milliliter63868-33114a76acf-da72-41b4-81fc-0d907b9fe63c12014-10-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1
AMMONIAINACTIVE INGREDIENT5138Q19F1X1
IODINEINACTIVE INGREDIENT9679TC07X41
POTASSIUM IODIDEINACTIVE INGREDIENT1C4QK22F9J1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63868-33163868-331-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMMONIA5138Q19F1XIACT
IODINE9679TC07X4IACT
POTASSIUM IODIDE1C4QK22F9JIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 6 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
AMMONIAAMMONIA SOLUTION5138Q19F1XGEL / TOPICAL1.2 %w/wExact identifier — unii+route
6 equally ranked IID candidates
AMMONIAAMMONIA SOLUTION5138Q19F1XLOTION / TOPICALADJ PHExact identifier — unii+route
6 equally ranked IID candidates
AMMONIAAMMONIA SOLUTION5138Q19F1XGEL / TOPICAL1.2 %w/wExact identifier — unii+route
6 equally ranked IID candidates
AMMONIAAMMONIA SOLUTION5138Q19F1XCREAM / TOPICAL5.72 %w/wExact identifier — unii+route
6 equally ranked IID candidates
AMMONIAAMMONIA SOLUTION5138Q19F1XCREAM / TOPICAL5.72 %w/wExact identifier — unii+route
6 equally ranked IID candidates
AMMONIAAMMONIA SOLUTION5138Q19F1XLOTION / TOPICALADJ PHExact identifier — unii+route
6 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Quality Choice Iodides TinctureETHYL ALCOHOLChain Drug Market Association71aedfd5-e81f-4b69-b163-527ff1ce30b12023-12-20WarningsExact identifier
ndc (package): 63868-331-02
ndc (product): 63868-331
ndc11 (package): 63868033102
spl id: 0cf4bfe6-384f-e836-e063-6394a90ab8c3
spl set id: 71aedfd5-e81f-4b69-b163-527ff1ce30b1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.