FDA.reportPublic FDA data

QC Iodine Tincture Mild

Manufacturer
Navarro Discount Pharmacies, LLC | Humco Holding Group, Inc | Humco Holding Group, Inc.
Effective date
2017-11-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:10:21

Label at a glance#

ProductQC Iodine Tincture Mild
Active ingredientIODINE, SODIUM IODIDE, ALCOHOL
Label structure13 sections

Dosage and administration

clean the affected area apply a small amount on the area 1 to 3 times daily may be covered with sterile bandage if bandaged let dry first

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Iodine 2%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Iodide 2.4%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 47%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Indications

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
  • Flammable: Keep away from sparks heat and flame

Stop use and consult doctor if

OTC - STOP USE SECTION

  • the condition persists or gets worse, or if using for longer than one 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 reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, give milk then a starch solution made by mixing two tablespoonfuls of cornstarch or flour to a pint of water. Contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the affected area
  • apply a small amount on the area 1 to 3 times daily
  • may be covered with sterile bandage
  • if bandaged let dry first

Other information

OTHER SAFETY INFORMATION

  • will stain skin and clothing

Inactive ingredient

INACTIVE INGREDIENT SECTION

Purified Water

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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
59970-21359970-213-91

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
IODINE9679TC07X4ACTIB
SODIUM IODIDEF5WR8N145CACTIM
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

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
5d68a002-3cc8-b2ce-e053-2991aa0a98c95d690d82-e4f7-57ad-e053-2a91aa0a38ea2017-11-07WarningsExact identifier
spl id: 5d68a002-3cc8-b2ce-e053-2991aa0a98c9
spl set id: 5d690d82-e4f7-57ad-e053-2a91aa0a38ea

Reported adverse events (FAERS/openFDA)#

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