FDA label 2528efb9-acfb-af0a-e063-6394a90aa941

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)

SPL set ID: fe39836b-97db-4472-a1d9-582152443dfa
SPL ID: 2528efb9-acfb-af0a-e063-6394a90aa941
Version: 13
Effective date: 2024-10-23
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:44:44

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 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		2528efb9-acfb-af0a-e063-6394a90aa941	id
spl set id		fe39836b-97db-4472-a1d9-582152443dfa	set_id

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

Do not use if you have difficulty swallowing in children under 6 years of age if you are pregnant for a period longer than week if you are bedridden or aged

Adverse reactions cross-check#

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

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

Adverse Reactions *This product is not manufactured or distributed by Roberts Pharmaceutical Corp., distributor of Robrts Mineral Oil. Disributed by DZA Brands, LLC 2110 Excutive Drive, Salisburg, NC 28147 For product questions or comments contact us at 1-866-322-2439 Please include UPC and code from the package.

Reported adverse events (FAERS/openFDA)#

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