Label: SCARLET OIL solution
- NDC Code(s): 58829-259-01, 58829-259-16
- Packager: FIRST PRIORITY INCORPORATED
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated June 5, 2023
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- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS:
- DIRECTIONS FOR USE:
- CAUTION:
- ACTIVE INGREDIENT:
- INACTIVE INGREDIENTS:
- WARNING:
- STORAGE:
- WARNINGS AND PRECAUTIONS
- Net Contents:
- INFORMATION FOR OWNERS/CAREGIVERS
- Net Contents: 16 fl oz (473 mL)
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INGREDIENTS AND APPEARANCE
SCARLET OIL
scarlet oil solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:58829-259 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 2.5 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58829-259-16 12 in 1 CASE 1 473 mL in 1 BOTTLE 2 NDC:58829-259-01 4 in 1 CASE 2 3785 mL in 1 JUG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/14/2012 Labeler - FIRST PRIORITY INCORPORATED (179925722)