Label: SODIUM SALICYLATE solution
- NDC Code(s): 51072-038-01
- Packager: Aurora Pharmaceutical, Inc.
- Category: OTC ANIMAL DRUG LABEL
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Drug Label Information
Updated December 2, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DESCRIPTION
- CALF LABEL CLAIM
- SWINE AND POULTRY LABEL CLAIM
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DIRECTIONS FOR USE
For Analgesic and Antipyretic Use
For Anti-Inflammatory/Anti-Prostaglandin Use - Day 1
- Warning
- Storage
- FOOD SAFETY WARNING
- Caution
- KEEP OUT OF REACH OF CHILDREN
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 3.79 Liters Bottle Label
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INGREDIENTS AND APPEARANCE
SODIUM SALICYLATE
sodium salicylate solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:51072-038 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM SALICYLATE (UNII: WIQ1H85SYP) (SALICYLIC ACID - UNII:O414PZ4LPZ) SODIUM SALICYLATE 48.6 g in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51072-038-01 3790 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/16/2011 Labeler - Aurora Pharmaceutical, Inc. (832848639) Establishment Name Address ID/FEI Business Operations Aurora Pharmaceutical, Inc. 832848639 MANUFACTURE