SODIUM SUFIDE- ingrown toenail pain relief kit gel 
Walgreens Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Ingrown Toenail Relief

Active ingredient

Sodium Sufide 1%

Purpose

Ingrown Toenail Pain Reliever

Use

For external use only.

Do not use

on open sores.

Ask a doctor before use if you have

  • diabetes
  • poor blood circulation
  • gout

When using this product

  • 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

  • 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

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

Directions

adults and children 12 yers and over:

Children under 12 years: ask a doctor

Other Information

Inactive Ingredient

edetate disodium, hydroxyethyl cellulose, pottasium acetate, water

Questions?

Call 1-866-964-0939

Principal Display Panel

Well at Walgreens

Ingrown Toenail Relief

Sodium Sulfide Gel 1%

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.jpg

SODIUM SUFIDE 
ingrown toenail pain relief kit gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9560
Route of AdministrationTopical
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SULFIDE (UNII: YGR27ZW0Y7) (SULFIDE ION - UNII:G15I91XETI) SODIUM SULFIDE0.085 g  in 8.5 g
Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM (UNII: 7FLD91C86K)  
POTASSIUM ACETATE (UNII: M911911U02)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-9560-858.5 g in 1 PACKAGE; Type 0: Not a Combination Product03/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358D03/01/2018
Labeler - Walgreens Company (008965063)

Revised: 3/2017
Document Id: 50bb5c9f-072a-478f-9c42-bbd04e20d49b
Set id: 5e081d6c-0619-4d6c-be50-588c488404eb
Version: 1
Effective Time: 20170317
 
Walgreens Company