Sunmark Mineral Oil Laxative

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: Sunmark Mineral Oil Laxative
Generic name: MINERAL OIL
Manufacturer: Strategic Sourcing Services
Product type: HUMAN OTC DRUG
SPL set ID: c54f7df2-3845-425f-b13e-3dc000123f3c
SPL ID: fdbfcdfe-c67a-4aa5-9dc5-f4bd11a51a53
Version: 5
Effective date: 2025-01-14
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:53:54

Harmonized routes table
Harmonized routes
RECTAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M007	openfda.application_number
brand name		Sunmark Mineral Oil Laxative	openfda.brand_name
generic name		MINERAL OIL	openfda.generic_name
manufacturer name		Strategic Sourcing Services	openfda.manufacturer_name
ndc	package	49348-185-20	openfda.package_ndc
ndc	product	49348-185	openfda.product_ndc
ndc11	package	49348018520	derived:openfda.package_ndc
rxcui		205121	openfda.rxcui
spl id		fdbfcdfe-c67a-4aa5-9dc5-f4bd11a51a53	id
spl set id		c54f7df2-3845-425f-b13e-3dc000123f3c	set_id
unii		T5L8T28FGP	openfda.unii

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 For rectal use only. Ask a doctor before use if you have abdominal pain, nausea, or vomiting a sudden change in bowel habits lasting more than 2 weeks already used a laxative for more than 1 week Stop use and ask a doctor if you have: rectal bleeding no bowel movement after use These symptoms may indicate a serious condition. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away: 800-222-1222.

Reported adverse events (FAERS/openFDA)#

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