Label: GERICARE SENNA SYRUP- sennosides liquid
- NDC Code(s): 57896-472-08
- Packager: Geri-Care Pharmaceutical Corp.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 13, 2022
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
Do not use
- laxative products for longer than 1 week unless directed by a doctor.
Ask a doctor or pharmacis before use if you have
- stomach pain, nausea or vomiting
- noticed a change in bowel habits that lasts over two weeks.
Stop use and ask a doctor if
you have rectal bleeding or failure to have a bowel movement after use of a laxative. These may indicate a serious condition.
- KEEP OUT OF REACH OF CHILDREN
DOSAGE & ADMINISTRATION
- Shake well before using
- Do not exceed recommended dose
Age Starting Dose Maximum Dose adults and children 12 years and older 2-3 teaspoonfuls once a day preferably at bedtime; increase as needed or as recommended by a doctor 3 teaspoons in the morning and 3 teaspoons at bedtime Under 12 years of age ask a doctor ask a doctor
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
GERICARE SENNA SYRUP
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57896-472 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 8.8 mg in 5 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:57896-472-08 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 04/13/2022 Labeler - Geri-Care Pharmaceutical Corp. (611196254)