Label: DE LA CRUZ CASTOR OIL- castor oil oil
- NDC Code(s): 24286-1526-5, 24286-1526-8, 24286-1526-9
- Packager: DLC Laboratories, Inc.
- 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.
Drug Label Information
Updated July 5, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- 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.
- for periods longer than a week. Frequent or prolonged use may result in dependence on laxatives.
Ask a doctor before use if you have noticed a sudden change in bowel habits that persists over a period of two weeks.
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Directions
Preferably taken on an empty stomach.
May be taken with juice to improve the taste.
Age Dose Adults and children 12 years and over 1 to 4 tablespoons in a single daily dose or as directed by a doctor Children 2 to under 12 years 1 to 3 teaspoons in a single daily dose or as directed by a doctor Children under 2 years Consult a doctor - Other information
- Questions
- SPL UNCLASSIFIED SECTION
- INACTIVE INGREDIENT
- Inactive ingredient
- PRINCIPAL DISPLAY PANEL - 59 mL Bottle Label
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INGREDIENTS AND APPEARANCE
DE LA CRUZ CASTOR OIL
castor oil oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24286-1526 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CASTOR OIL (UNII: D5340Y2I9G) (CASTOR OIL - UNII:D5340Y2I9G) CASTOR OIL 1 g in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24286-1526-5 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/27/2012 2 NDC:24286-1526-8 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/03/2022 3 NDC:24286-1526-9 236 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/03/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 07/27/2012 Labeler - DLC Laboratories, Inc. (093351930) Establishment Name Address ID/FEI Business Operations DLC Laboratories, Inc. 093351930 manufacture(24286-1526) , label(24286-1526)
