Label: HYPERTONIC SALINE injection, solution
- NDC Code(s): 57319-554-08
- Packager: Phoenix
- Category: PRESCRIPTION ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated January 29, 2018
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- INDICATIONS:
- CAUTION:
- DOSAGE AND ADMINISTRATION:
- VETERINARY INDICATIONS
- WARNINGS AND PRECAUTIONS
- CAUTION:
- COMPOSITION:
- STORAGE AND HANDLING
- GENERAL PRECAUTIONS
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INFORMATION FOR OWNERS/CAREGIVERS
Manufactured by
Nova-Tech, Inc.
Grand Island, NE 68801RMS 92-548
18-806-60
Rev. 06-10
NDC 57319-554-08
Sterile - Preservative Free
Net Contents: 1000 mL
Manufactured for:
Clipper Distributing Company, LLC
St. Joseph, MO 64507Trademarks are property of
Clipper Distributing Company, LLCLot No.
Exp. Date
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HYPERTONIC SALINE
hypertonic saline injection, solutionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:57319-554 Route of Administration INTRAVENOUS, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 7.2 g in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57319-554-08 1000 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/16/2018 Labeler - Phoenix (150711039) Registrant - Phoenix (150711039) Establishment Name Address ID/FEI Business Operations Nova-Tech, Inc. 196078976 manufacture, api manufacture