De La Cruz Castor Oil

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
De La Cruz Castor Oil
Generic name
CASTOR OIL
Manufacturer
DLC Laboratories, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
22fbad2e-e9fa-46ba-8617-ad79483cbe9a
SPL ID
377a5b4a-a015-ee13-e063-6394a90a2950
Version
14
Effective date
2025-06-13
Source export date
2026-11-06
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:02:35
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

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.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.