Label: ASPEN ASPIRIN LIQUID CONCENTRATE- aspirin liquid concentrate liquid
- NDC Code(s): 65090-111-32
- Packager: AHC Products Inc
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated July 10, 2023
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WARNINGS AND PRECAUTIONS
For Animal Use Only
Keep Out of Reach of Children
Solo Para Uso Animal
Mantenga Fuera del Alcanze de los NinosWARNINGS: FOR ANIMAL USE ONLY. KEEP OUT OF THE REACH OF CHILDREN. SHAKE WELL BEFORE USE. FLAMMABLE-USE WITH CAUTION.
ADVERTENCIA: ANIMAL SOLO PARA USO. Mantener fuera del alcance de los ninos. AGITAR BIEN ANTES DE SU USO. INFLAMABLES: USO CON PRECAUCION.
- INDICATIONS & USAGE
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DOSAGE & ADMINISTRATION
One ounce of Aspirin Liquid Concentrate to one gallon of water. Stir solution and meter with proportioner at the rate of 1:128 gallons. For seven day continuous rate use four ounces of Aspirin Liquid Concentrate to one gallon of water on day one and one ounce of Aspirin Liquid Concentrate to one gallon of water for the remaining six days.
Keep container securely closed when not in use. Store in a cool, dry place.
Una onza de Aspirina Liquida Concentrada para un galon de agua. Agitar la solucion y medidor con dosificador a una tasa de 1:128 galones. Para siete dias continuos tasa utilizar cuatro onzas de Aspirina Liquida Concentrada para un galon de agua en el primer dia y una onza de Aspirina Liquida Concentrada para un galon de agua para los restantes sies dias.
Conservese el recipiente cerrado de forma segura cuando no este en uso. Almacenar en un lugar fresco y seco. - ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ASPEN ASPIRIN LIQUID CONCENTRATE
aspirin liquid concentrate liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:65090-111 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 120 mg in 1 mL Inactive Ingredients Ingredient Name Strength FD&C BLUE NO. 1 (UNII: H3R47K3TBD) 1300 ng in 1 mL GLYCERIN (UNII: PDC6A3C0OX) 4.9 mg in 1 mL PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 139 mg in 1 mL ALCOHOL (UNII: 3K9958V90M) 706 mg in 1 mL ETHYL ACETATE (UNII: 76845O8NMZ) 30 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65090-111-32 946 mL in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/01/2015 Labeler - AHC Products Inc (169764193) Establishment Name Address ID/FEI Business Operations Shandong Xinhua Pharmaceutical Co., Ltd. 421252895 api manufacture Establishment Name Address ID/FEI Business Operations AHC Products Inc 169764193 manufacture