Label: ALOPHEN- bisacodyl tablet, coated
- NDC Code(s): 69846-140-01
- Packager: NUMARK BRANDS, INC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 18, 2023
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- ACTIVE INGREDIENT
- Use
- Warnings
- Ask a doctor before use if you have
- When using this product
- Stop use and ask a doctor if
- PREGNANCY OR BREAST FEEDING
- Keep out of reach of children.
- Directions
- Other information
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Inactive ingredients
acacia, ammonium hydroxide, calcium carbonate, carnauba wax, colloidal anhydrous silica, corn starch, D&C yellow #10 aluminum lake, FD&C yellow #6 aluminum lake, hypromellose, iron oxide black, lactose anhydrous, magnesium stearate, methylparaben, polydextrose, polyethylene glycol, polyvinyl acetate phthalate, povidone, propylene glycol, propylparaben, shellac glaze, simethicone, sodium alginate, sodium benzoate, sodium bicarbonate, stearic acid, sucrose, talc, titanium dioxide, triacetin, triethyl citrate
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PRINCIPAL DISPLAY PANEL
NDC 69846-140-01
Now Smaller,
Easier to Swallow
Alophen®
(Bisacodyl USP)
Comfort Coated
Stimulant Laxative
Gentle, Effective
Overnight Relief
100 Tablets, 5 mg. each
Do not use if printed "SEALED FOR YOUR PROTECTION" inner seal is broken or missing.
Dist. by: Numark Brands, Inc. 57001
EDISON, NJ 08818 1-800-214-2379 Rev. 4/21
LOT #
EXP. DATE
NDC 69846-140-01
Now Smaller, Easier to Swallow
Alophen®
(Bisacodyl USP)
Comfort Coated
Stimulant Laxative
Gentle, Effective
Overnight Relief
100 Tablets, 5 mg. each
REFER TO OUTER CARTON FOR FULL INFORMATION
Distributed by: Numark Brands, Inc.
EDISON, NJ 08818 1-800-214-2379 57000 Rev. 1/21
LOT #
EXP. DATE
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INGREDIENTS AND APPEARANCE
ALOPHEN
bisacodyl tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69846-140 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Bisacodyl (UNII: 10X0709Y6I) (Deacetylbisacodyl - UNII:R09078E41Y) Bisacodyl 5 mg Inactive Ingredients Ingredient Name Strength Acacia (UNII: 5C5403N26O) Ammonia (UNII: 5138Q19F1X) Calcium Carbonate (UNII: H0G9379FGK) Carnauba Wax (UNII: R12CBM0EIZ) Silicon Dioxide (UNII: ETJ7Z6XBU4) Starch, Corn (UNII: O8232NY3SJ) D&C Yellow No. 10 (UNII: 35SW5USQ3G) Fd&C Yellow No. 6 (UNII: H77VEI93A8) Hypromellose, Unspecified (UNII: 3NXW29V3WO) Ferrosoferric Oxide (UNII: XM0M87F357) Anhydrous Lactose (UNII: 3SY5LH9PMK) Magnesium Stearate (UNII: 70097M6I30) Methylparaben (UNII: A2I8C7HI9T) Polydextrose (UNII: VH2XOU12IE) Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A) Polyvinyl Acetate Phthalate (UNII: 58QVG85GW3) Povidone, Unspecified (UNII: FZ989GH94E) Propylene Glycol (UNII: 6DC9Q167V3) Propylparaben (UNII: Z8IX2SC1OH) Shellac (UNII: 46N107B71O) Dimethicone (UNII: 92RU3N3Y1O) Sodium Alginate (UNII: C269C4G2ZQ) Sodium Benzoate (UNII: OJ245FE5EU) Sodium Bicarbonate (UNII: 8MDF5V39QO) Stearic Acid (UNII: 4ELV7Z65AP) Sucrose (UNII: C151H8M554) Talc (UNII: 7SEV7J4R1U) Titanium Dioxide (UNII: 15FIX9V2JP) Triacetin (UNII: XHX3C3X673) Triethyl Citrate (UNII: 8Z96QXD6UM) Product Characteristics Color YELLOW, ORANGE Score no score Shape ROUND Size 6mm Flavor Imprint Code TCL;003 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69846-140-01 1 in 1 CARTON 04/15/1907 1 100 in 1 BOTTLE, PLASTIC; 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 04/15/1907 06/01/2024 Labeler - NUMARK BRANDS, INC (080184668)