Label: PERCY MEDICINE- bismuth subsalicylate liquid
- NDC Code(s): 0322-2222-00, 0322-2222-03
- Packager: Merrick Medicine Company, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 15, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts Active Ingredient
- Purpose
-
Warnings
Children and teenagers that have or are recovering from Chicken Pox, flu systems, or flue should NOT use this product. If nausea, vomiting, or fever occur, consult a doctor because these symptoms could be an early sign of Reye Syndrome, a rare but serious condition.
Allergy Alert: Contains Salicylates. Do Not take if you are - allergic to salicylates (including aspirin) - taking other salicylate products.
Do not use if you have - blood or black stool - an ulcer - bleeding problem.
Ask a doctor before use if you are taking any drug for anti coagulation (thinning of the blood), diabetes,gout, arthritis. - When using this product a temporary but harmless darkening of the stool and/or tongue may occur.
Stop use and consult a doctor if - symptoms get worse - ringing in the ears or loss of hearing occurs - diarrhea lasts more that 2 days.
if pregnant or breast feeding ask a professional before use. In case of accidental overdose, get medical help or contact a Poison Control Center immediately.
- Inactive Ingredients
- Directions
- Keep out of reach of children
- Uses:
- Package Label
-
INGREDIENTS AND APPEARANCE
PERCY MEDICINE
bismuth subsalicylate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0322-2222 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ) BISMUTH SUBSALICYLATE 1050 mg in 10 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CALCIUM HYDROXIDE (UNII: PF5DZW74VN) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) ACACIA (UNII: 5C5403N26O) ORANGE OIL (UNII: AKN3KSD11B) CINNAMON OIL (UNII: E5GY4I6YCZ) POTASSIUM CARBONATE (UNII: BQN1B9B9HA) RHUBARB (UNII: G280W4MW6E) SUCROSE (UNII: C151H8M554) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0322-2222-00 1 in 1 BOX 09/09/2019 1 NDC:0322-2222-03 90 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:0322-2222-03 90 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/09/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M008 09/09/2019 Labeler - Merrick Medicine Company, Inc (007331838) Registrant - Pharma Nobis, LLC (118564114) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 analysis(0322-2222) , manufacture(0322-2222) , pack(0322-2222) , label(0322-2222)
