DE LA CRUZ CASTOR OIL- castor oil oil 
DLC Laboratories, Inc.

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CASTOR OIL

Drug Facts

Active ingredient

Castor oil, USP 100%

Purpose

Stimulant laxative

Uses

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.

Ask a doctor or pharmacist before use if you are taking any other drug.

Stop use and ask a doctor if you have rectal bleeding or failure to have a bowel movement after use of a laxative. These symptoms may indicate a serious condition.

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center immediately.

Directions

Preferably taken on an empty stomach.

May be taken with juice to improve the taste.

AgeDose
Adults and children 12 years and over1 to 4 tablespoons in a single daily dose or as directed by a doctor
Children 2 to under 12 years1 to 3 teaspoons in a single daily dose or as directed by a doctor
Children under 2 yearsConsult a doctor

Other information

Storage

Keep tightly closed and away from excessive heat.

Questions

1-800-858-3889
www.dlclabs.com

Distributed by:
De La Cruz Products
A Division of DLC Laboratories, Inc.
Paramount, CA 90723 USA

none

Inactive ingredient

none

PRINCIPAL DISPLAY PANEL - 59 mL Bottle Label

De La Cruz ®

CASTOR

OIL


USP

Stimulant Laxative

2 FL OZ (59 mL)

DLC-Castor-Oil-8

castor oil 2 oz

DE LA CRUZ CASTOR OIL 
castor oil oil
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1526
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CASTOR OIL (UNII: D5340Y2I9G) (CASTOR OIL - UNII:D5340Y2I9G) CASTOR OIL1 g  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1526-559 mL in 1 BOTTLE; Type 0: Not a Combination Product07/27/2012
2NDC:24286-1526-8236 mL in 1 BOTTLE; Type 0: Not a Combination Product08/03/2022
3NDC:24286-1526-9236 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product08/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00707/27/2012
Labeler - DLC Laboratories, Inc. (093351930)
Establishment
NameAddressID/FEIBusiness Operations
DLC Laboratories, Inc.093351930manufacture(24286-1526) , label(24286-1526)

Revised: 5/2024
Document Id: 177f48c4-abea-dcde-e063-6294a90a16dc
Set id: 22fbad2e-e9fa-46ba-8617-ad79483cbe9a
Version: 12
Effective Time: 20240502
 
DLC Laboratories, Inc.