Country: United States
Language: English
Source: NLM (National Library of Medicine)
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)
Scholls Wellness Company LLC
TOPICAL
OTC DRUG
Corn remover Uses for the removal of corns relieves pain by removing corns Do not use if you are a diabetic if you have poor blood circulation on irritated skin or any area that is infected or reddened
OTC monograph final
SCHOLLS WELLNESS COMPANY LLC CORN REMOVERS- SALICYLIC ACID DISC SCHOLLS WELLNESS COMPANY LLC _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._ ---------- CORN REMOVERS DRUG FACTS Drug Facts Active Ingredient Purpose Salicylic Acid 40%.......................Corn remover PURPOSE Corn remover USES Uses for the removal of corns relieves pain by removing corns Warnings For external use only Do not use if you are a diabetic if you have poor blood circulation on irritated skin or any area that is infected or reddened Stop use and ask a doctor if discomfort lasts Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. DIRECTIONS DURAGEL CORN CALLUS REMOVER Directions wash affected area and dry thoroughly if necessary, cut medicated disc to fit corn apply medicated disc with sticky side adhering to skin cover medicated disc with enclosed cushion after 48 hours, remove medicated disc repeat procedure every 48 hours as needed for up to 14 days (until corn is removed) may soak callus in warm water for 5 minutes to assist in removal OTHER INFORMATION Other information store between 20ºC to 25ºC (68º to 77ºF). Inactive ingredients antioxidant (CAS 991-84-4), iron oxides, mineral oil, petroleum hydrocarbon resin, silicon dioxide, synthetic polyisoprene rubber, talc Questions? 1-866-360-3226 SCHOLLS WELLNESS COMPANY LLC CORN REMOVERS Scholls Wellness Company LLC salicylic acid disc PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:73469-0638 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.4 g in 1 g INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH MINERAL OIL (UNII: T5L8T28FGP) TALC (UNII: 7SEV7J4R1U) BROWN IRON OXIDE (UNII: 1N032N7MFO) PRODUCT CH Read the complete document