Label: DOCUSATE SODIUM capsule, liquid filled
-
NDC Code(s):
63739-478-01,
63739-478-02,
63739-478-10,
63739-478-40, view more63739-478-48
- Packager: McKesson Corporation
- This is a repackaged label.
- Source NDC Code(s): 61301-8001
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 11, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each capsule)
- Purpose
- Uses
-
Warnings
Do not use
- if you are currently taking mineral oil, unless directed by a doctor
- when abdominal pain, nausea, or vomiting are present
- for longer than 1 week unless directed by a doctor
Ask a doctor before use if you notice a sudden change in bowel habits that persists 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 use
If pregnant or breast-feeding, ask a health professional before use.
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- HOW SUPPLIED
- Docusate Sodium
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DOCUSATE SODIUM
docusate sodium capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63739-478(NDC:61301-8001) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 100 mg Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SORBITOL (UNII: 506T60A25R) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) WATER (UNII: 059QF0KO0R) GELATIN, UNSPECIFIED (UNII: 2G86QN327L) FD&C RED NO. 40 (UNII: WZB9127XOA) Product Characteristics Color red (Reddish) Score no score Shape OVAL Size 12mm Flavor Imprint Code SCU1 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63739-478-01 25 in 1 BOX, UNIT-DOSE 11/09/2010 02/28/2016 1 30 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:63739-478-10 10 in 1 BOX, UNIT-DOSE 11/09/2010 02/28/2016 2 10 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:63739-478-48 1000 in 1 BOTTLE; Type 0: Not a Combination Product 09/19/2017 09/21/2017 4 NDC:63739-478-40 100 in 1 BOTTLE; Type 0: Not a Combination Product 09/19/2017 09/21/2017 5 NDC:63739-478-02 30 in 1 BOX, UNIT-DOSE 07/01/2021 5 10 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 505G(a)(3) 11/09/2010 Labeler - McKesson Corporation (140529962) Registrant - McKesson Corporation dba SKY Packaging (140529962) Establishment Name Address ID/FEI Business Operations Contract Packaging Resources Inc. 960203917 repack(63739-478)
