FDA.reportPublic FDA data

Sodium Sufide

Manufacturer
Walgreens Company
Effective date
2017-03-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:45

Label at a glance#

ProductSodium Sufide
Active ingredientSODIUM SULFIDE
Label structure9 sections

Dosage and administration

adults and children 12 yers and over: wash affected area and dry thoroghly place retainer ring on toe with slot over the area where the ingrown nail and the skin meet. Smooth ring down firmly cut open tip of the tube on score mark. Apply enough gel prodcut to fill the slot in the ring. Immeciately replace cap on tube place round center section of bandage directly over the gel- filled ring to seal the gel in place....

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Sufide 1%

Purpose

OTC - PURPOSE SECTION

Ingrown Toenail Pain Reliever

Use

INDICATIONS & USAGE SECTION

  • for the temporary releif of pain and discomfort from ingrown toenails

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on open sores.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • diabetes
  • poor blood circulation
  • gout

When using this product

OTC - WHEN USING SECTION

  • use with a retainer ring
  • avoid contact with eyes. If prodcut gets into the eye, flush with water for 15 minutes and get medical help reight away.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • redness or swelling of your toe increases
  • discharge is present around the nail
  • symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 12 yers and over:

  • wash affected area and dry thoroghly
  • place retainer ring on toe with slot over the area where the ingrown nail and the skin meet. Smooth ring down firmly
  • cut open tip of the tube on score mark. Apply enough gel prodcut to fill the slot in the ring. Immeciately replace cap on tube
  • place round center section of bandage directly over the gel- filled ring to seal the gel in place. Smooth ends of bandage strips around toe
  • repeat twice daily (morning and night) for up to 7 days until pain discomfort is relieved or until the nail can be lifted out of the nail groove and easliy trimmed

Children under 12 years: ask a doctor

Other Information

OTHER SAFETY INFORMATION

  • save carton for complete warnings and information
  • keep tube tightly closed when not in use
  • store between 68o anf 77oF (20o and 25oC)

Inactive Ingredient

INACTIVE INGREDIENT SECTION

edetate disodium, hydroxyethyl cellulose, pottasium acetate, water

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Well at Walgreens

Ingrown Toenail Relief

Sodium Sulfide Gel 1%

  • Relieves ingrown toenail pain
  • Softens nail 
  • Cushions & protects afftected area

12APPLICATIONS

12 RETAINER RING CUSHIONS

12 BANDAGES

1 TUBE OF TREATMENT GEL

NET WT 8.5 g(0.3 OZ)

Walgreens Ingrown Toenail_53-158WG.jpgWalgreens Ingrown Toenail_53-158WG.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1293723sodium sulfide 1 % Topical GelPSN1
1293723sodium sulfide 0.01 MG/MG Topical GelSCD1
1293723sodium sulfide 1 % Topical GelSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d9771140-739b-484b-ae64-b79528ff1211Product name320250801

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-9560-852021-07-23C16284748780-1c7ccaba7-27a8-fd44-e053-dadaa90aa01bIngrown Toenail Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-9560-85Sodium Sufide8.5 g in 1 PACKAGEGEL8.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-9560SODIUM SUFIDE (INGROWN TOENAIL PAIN RELIEF KIT) GEL [WALGREENS COMPANY]1Legacy NDC, 1 package rows20180301_5e081d6c-0619-4d6c-be50-588c488404eb.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
0363-95600363-9560-85

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
SODIUM SULFIDEYGR27ZW0Y7ACTIB
EDETATE DISODIUM7FLD91C86KIACT
POTASSIUM ACETATEM911911U02IACT
WATER059QF0KO0RIACT

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
50bb5c9f-072a-478f-9c42-bbd04e20d49b5e081d6c-0619-4d6c-be50-588c488404eb2017-03-17WarningsExact identifier
spl id: 50bb5c9f-072a-478f-9c42-bbd04e20d49b
spl set id: 5e081d6c-0619-4d6c-be50-588c488404eb

Reported adverse events (FAERS/openFDA)#

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