Mineral 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
Mineral Oil
Generic name
MINERAL OIL
Manufacturer
Publix Supermarkets, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
382a57d1-85bf-480f-9967-f85da2904410
SPL ID
9080dcf0-1706-480f-b1d1-f6215099da4e
Version
6
Effective date
2026-04-23
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:43:50
Harmonized routes table
Harmonized routes
ORAL, TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not use in children under 6 years of age, pregnant wormen, bedridden patients or persons with difficulty swallowing if you are presently taking a stool softener laxative for longer than 1 week unless directed by a doctor Ask a doctor before use if you have abdominal pain, nausea or vomiting noticed a sudden change in bowel habits that persists over a period of 2 weeks When using this product do not take with meals take only at bedtime Stop use and ask a doctor if you have rectal bleeding or failure to have a bowel movement after use. These could be signs of a serious condition. If pregnant or breast feeding, ask a health professional before use. As with any drug, if you are nursing a baby, seek the advice of a health professional before using this product. Keep out of reach of children In case of overdose, get medical help or contact a Poison Control center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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