Label: SENNA syrup
- NDC Code(s): 68094-049-59, 68094-049-62
- Packager: Precision Dose, Inc.
- This is a repackaged label.
- Source NDC Code(s): 71399-0027
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 5, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each teaspoonful)
- Purpose
- Uses
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Warnings
ask a doctor before use if you have
- stomach pain
- nausea
- vomiting
- noticed a sudden change in bowel movements that continues over a period of 2 weeks
Ask a doctor or pharmacist before use if you are taking any other drug. Take this product two or more hours before or after other drugs. Laxatives may affect how other drugs work.
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Directions
take preferably at bedtime or as directed by a doctor. Shake Well Before Using.
age starting dose maximum dosage Adults and children 12 years and older 2-3 teaspoons once a day 3 teaspoons twice a day Children 6 years to under 12 years 1-1½ teaspoons once a day 1½ teaspoons twice a day Children 2 years to under 6 years ½ - ¾ teaspoon once a day ¾ teaspoon twice a day Children under 2 years ask a doctor ask a doctor - Other information
- Inactive ingredients
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- How Supplied
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 5 mL Cup Label
-
INGREDIENTS AND APPEARANCE
SENNA
senna syrupProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68094-049(NDC:71399-0027) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sennosides A and B (UNII: 1B5FPI42EN) (Sennosides A and B - UNII:1B5FPI42EN) Sennosides A and B 417.12 mg in 237 mL Inactive Ingredients Ingredient Name Strength Methylparaben (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) SUCROSE (UNII: C151H8M554) Product Characteristics Color Score Shape Size Flavor CHOCOLATE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68094-049-62 3 in 1 CASE 06/15/2024 1 10 in 1 TRAY 1 NDC:68094-049-59 5 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M007 06/15/2024 Labeler - Precision Dose, Inc. (035886746) Establishment Name Address ID/FEI Business Operations Precision Dose, Inc. 035886746 REPACK(68094-049)