Label: HEB MAXIMUM STRENGTH LAXATIVE PILLS- sennosides tablet
- NDC Code(s): 37808-149-12, 37808-149-27
- Packager: H E B
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 26, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT(in each tablet)
- PURPOSE
- USE(S)
- WARNINGS
- ASK A DOCTOR BEFORE USE IF YOU HAVE
- ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU
- WHEN USING THIS PRODUCT
- STOP USE AND ASK A DOCTOR IF
- IF PREGNANT OR BREASTFEEDING,
- KEEP OUT OF REACH OF CHILDREN
-
DIRECTIONS
- swallow tablet(s) with a glass of water
- swallow tablet(s) whole, do not crush, break or chew
adults and children 12 years and over take 2 tablets once or twice daily with a glass of water children 6 to under 12 years take 1 tablet once or twice daily with a glass of water children under 6 years ask a doctor
- OTHER INFORMATION
- INACTIVE INGREDIENT SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HEB MAXIMUM STRENGTH LAXATIVE PILLS
sennosides tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-149 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 25 mg Inactive Ingredients Ingredient Name Strength ACACIA (UNII: 5C5403N26O) ALGINIC ACID (UNII: 8C3Z4148WZ) CALCIUM SULFATE (UNII: WAT0DDB505) YELLOW WAX (UNII: 2ZA36H0S2V) CARNAUBA WAX (UNII: R12CBM0EIZ) CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561) ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) KAOLIN (UNII: 24H4NWX5CO) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) SODIUM BENZOATE (UNII: OJ245FE5EU) STARCH, CORN (UNII: O8232NY3SJ) SUCROSE (UNII: C151H8M554) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color BLUE Score no score Shape ROUND Size 9mm Flavor Imprint Code G177 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-149-27 6 in 1 CARTON 04/02/2018 1 15 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:37808-149-12 2 in 1 CARTON 04/02/2018 2 12 in 1 BLISTER PACK; 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 04/02/2018 Labeler - H E B (007924756) Establishment Name Address ID/FEI Business Operations Guardian Drug Company 119210276 MANUFACTURE(37808-149)