Label: SENNA syrup
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Contains inactivated NDC Code(s)
NDC Code(s): 71399-8237-8 - Packager: Akron Pharma Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 18, 2023
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- Active Ingredient
- Uses
- Directions
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DOSAGE & ADMINISTRATION
age starting dose maximum dosage Mulls and children 12 yeart and older 2-3 teaspoons once a day 3 teaspoons twice a day Children 6 years to under 12 yeart 1 -11> teaspoons once a day 11> teaspoons twice a day Children 2 yeart to under 6 yeart l> -¾teaspoon once a day ¾ teaspoon twice a day Children under 2 years ask a doctor ask a doctor - Warnings
- Other Information
- Inactive Ingredients
- KEEP OUT OF REACH OF CHILDREN SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SENNA
senna syrupProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71399-8237 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:71399-8237-8 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/25/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 10/25/2019 Labeler - Akron Pharma Inc. (067878881)