Label: BISMUTH SUSPENSION- bismuth subsalicylate suspension
- NDC Code(s): 13985-564-01
- Packager: MWI/Vet One
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 10, 2022
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- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS
- DOSAGE AND ADMINISTRATION:
- WARNING:
- CAUTION:
- WHEN USING
- ACTIVE INGREDIENT:
- INACTIVE INGREDIENTS:
- STORAGE:
- Net Contents:
- INFORMATION FOR OWNERS/CAREGIVERS
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INGREDIENTS AND APPEARANCE
BISMUTH SUSPENSION
bismuth subsalicylate suspensionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:13985-564 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ) BISMUTH SUBSALICYLATE 17.4 g in 1 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13985-564-01 4 in 1 CASE 1 3.785 L in 1 JUG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/13/2015 Labeler - MWI/Vet One (019926120) Establishment Name Address ID/FEI Business Operations First Priority Incorporated 179925722 manufacture, label, api manufacture