Label: SALICYLIC ACID- corn and callus remover liquid liquid
- NDC Code(s): 11822-0120-9
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only.
Flammable
- keep away from fire or flame
- cap bottle tightly and store at room temperature away from heat
Do not use
- on irritated skin
- on any area that is infected or reddened
- if you are a diabetic, or if you have poor blood circulation, except under the advice and supervision of a doctor or podiatrist
-
Directions
- wash the affected area and dry thoroughly
- apply one drop at a time with applicator to sufficiently cover each corn/callus; let dry
- use cushion with hole centered over corn or callus to relieve pressure (additional cushions may be purchased separately)
- repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)
- may soak corn/callus in warm water for 5 minutes to assist in removal
- Other information
- Inactive ingredients
- Questions?
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
SALICYLIC ACID
corn and callus remover liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0120 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.17 mg in 9.8 mL Inactive Ingredients Ingredient Name Strength PYROXYLIN (UNII: KYR8BR2X6O) CAMPHOR (NATURAL) (UNII: N20HL7Q941) CASTOR OIL (UNII: D5340Y2I9G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0120-9 9.8 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 12/22/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M030 12/22/2017 Labeler - Rite Aid Corporation (014578892)