Label: PUBLIX LAXATIVE MAXIMUM STRENGTH- calcium sennosides tablet
- NDC Code(s): 41415-114-24
- Packager: PUBLIX SUPER MARKETS, INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 7, 2023
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Do not use
laxative products when abdominal pain, nausea, or vomiting are present unless directed by a doctor.
Ask a doctor before use if you have
- ▪
- noticed a sudden change in bowel habits that persists over a period of 2 weeks.
Ask a doctor or pharmacist before use if you are
- •
- are taking a prescription drug. Laxatives may affect how other drugs work. Take this product 2 or more hours before or after other drugs.
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Directions
- ▪
- swallow pill(s) with a glass of water
- ▪
- swallow pill(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
take1 tablet once or twice daily with a glass of water
children under 6 years
ask a doctor
- Other information
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Inactive ingredients
acacia, calcium sulfate anhydrous, carnauba wax, colloidal silicon dioxide, corn starch, croscarmellose sodium, dibasic calcium phosphate dehydrate, FD&C Blue No. 1, iron oxide, iron oxide black, iron oxide yellow, kaolin, magnesium sterate, maltodextrin, microcrystalline cellulose, polyethylene glycol, povidone, shellac, stearic acid, sugar, talc, titanium dioxide.
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Principal Display Panel
*Compare to the active ingredient in EX-LAX® Maximum Strength Tablets
Publix®
NDC# 41415-114-24
MAXIMUM STRENGTH
LaxativeCALCIUM SENNOSIDES USP 25 mg/
STIMULANT LAXATIVE24 TABLETS
TAMPER EVIDENT: DO NOT USE IF ANY INDIVIDUAL BLISTER IS BROKEN OR OPEN.
DISTRIBUTED BY PUBLIX SUPER MARKETS, INC.,
3300 PUBLIX CORPORATE PARKWAY
LAKELAND, FL 33811
1-888-267-3037 publix.com
PUBLIX GUARANTEE: COMPLETE SATISFACTION OR YOUR MONEY BACK
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INGREDIENTS AND APPEARANCE
PUBLIX LAXATIVE MAXIMUM STRENGTH
calcium sennosides tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41415-114 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 25 mg Inactive Ingredients Ingredient Name Strength ACACIA (UNII: 5C5403N26O) CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H) CARNAUBA WAX (UNII: R12CBM0EIZ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STARCH, CORN (UNII: O8232NY3SJ) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) KAOLIN (UNII: 24H4NWX5CO) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) SHELLAC (UNII: 46N107B71O) STEARIC ACID (UNII: 4ELV7Z65AP) RAW SUGAR (UNII: 8M707QY5GH) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color BLUE Score no score Shape ROUND Size 10mm Flavor Imprint Code RP114 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41415-114-24 2 in 1 CARTON 05/15/2019 1 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 05/15/2019 Labeler - PUBLIX SUPER MARKETS, INC (006922009)