Label: DOCUZEN- sennosides 8.6mg and docusate sodium 50mg tablet
- NDC Code(s): 71574-700-60
- Packager: Village Pharma
- 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.
Updated November 27, 2018
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- Active Ingredients (in each tablet)
Do not use
- laxative products for longer than 1 week unless directed by a doctor
- if you are taking mineral oils, unlesss directed by a doctor
Ask a doctor before use if you have
- stomach pain
- noticed a sudden change in bowel habits that continues over a period of 2 weeks
Stop use and ask a doctor if
- you have rectal bleeding
- you fail to have a bowel movement after the use of a laxative.
These may indicate a serious condition.
- take preferably at bedtime or as directed by a doctor
Adults and children 12 years and over
2 tablets once a day
4 tablets twice a day
Children 6 to under 12 years
1 tablet once a day
2 tablets twice a day
Children 2 to under 6 years
1/2 tablet once a day
1 tablet twice a day
Children under 2 years
ask a doctor
ask a doctor
- Other information
- Inactive ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
sennosides 8.6mg and docusate sodium 50mg tablet
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71574-700 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 8.6 mg DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 50 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) SODIUM BENZOATE (UNII: OJ245FE5EU) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color orange (ORANGE COLOR) Score no score Shape ROUND (ROUND TABLET) Size 10mm Flavor Imprint Code PH32 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71574-700-60 60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/27/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 11/27/2018 Labeler - Village Pharma (080749749) Registrant - Village Pharma (080749749) Establishment Name Address ID/FEI Business Operations Pharbest Pharmaceuticals, Inc. 557054835 manufacture(71574-700) , pack(71574-700) , analysis(71574-700)