FDA.reportPublic FDA data

Sanar Naturals Decolorized Iodine

Manufacturer
Sanvall Enterprises, Inc | Evi Labs
Effective date
2024-10-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:32:26

Label at a glance#

ProductSanar Naturals Decolorized Iodine
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

first aid antiseptic to help prevent infection in minor cuts, scrapes and burns

Dosage and administration

Clean affected area Apply a small amount to the affected area 1 to 3 times daily

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 45%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

first aid antiseptic to help prevent infection in minor cuts, scrapes and burns

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from spark, heat or flame

Ask a doctor before use

OTC - ASK DOCTOR SECTION

if you have

  • deep puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition persists or gets worse

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. Donot apply over large areas of the body.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of ingestion, seek medical attention or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean affected area
  • Apply a small amount to the affected area 1 to 3 times daily

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, ammonia solution, iodine, potassium iodide

Label copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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
73386-147-01Sanar Naturals Decolorized Iodine30 g in 1 BOTTLELIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73386-147SANAR NATURALS DECOLORIZED IODINE (ETHYL ALCOHOL) LIQUID [SANVALL ENTERPRISES, INC]2Current NDC, 1 package rows20241102_16c92427-84d2-cad5-e063-6394a90af435.zip

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
73386-14773386-147-01

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
WATER059QF0KO0RIACT
AMMONIA5138Q19F1XIACT
IODINE9679TC07X4IACT
ALCOHOL3K9958V90MACTIB
POTASSIUM IODIDE1C4QK22F9JIACT

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
Sanar Naturals Decolorized IodineETHYL ALCOHOLSanvall Enterprises, Inc16c92427-84d2-cad5-e063-6394a90af4352024-10-31WarningsExact identifier
ndc (package): 73386-147-01
ndc (product): 73386-147
ndc11 (package): 73386014701
spl id: 25ca58e2-5188-6f74-e063-6294a90a35c0
spl set id: 16c92427-84d2-cad5-e063-6394a90af435

Reported adverse events (FAERS/openFDA)#

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