Label: PROMOLAXIN- docusate sodium tablet
- NDC Code(s): 27495-012-01
- Packager: Physicians Science & Nature Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 14, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
- Ask a doctor before use if you have
- Stop use and ask a doctor if
- If pregnant or breast-feeding,
- Keep out of Reach of Children.
- Directions
- Other information
- Inactive ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
PROMOLAXIN
docusate sodium tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:27495-012 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 HYPROMELLOSES (UNII: 3NXW29V3WO) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) STARCH, CORN (UNII: O8232NY3SJ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM BENZOATE (UNII: OJ245FE5EU) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white Score no score Shape ROUND Size 11mm Flavor Imprint Code GPI;S1 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:27495-012-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 04/15/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 04/15/2011 Labeler - Physicians Science & Nature Inc. (012485755) Establishment Name Address ID/FEI Business Operations Gemini Pharmaceuticals 055942270 manufacture(27495-012)