Stratuscare Adult Glycerin

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: Stratuscare Adult Glycerin
Generic name: GLYCERIN
Manufacturer: Stratus Pharmaceuticals
Product type: HUMAN OTC DRUG
SPL set ID: 3e1935da-5c1f-4942-98dd-320fade82321
SPL ID: 14962a4b-8181-4cb7-ab2b-79877d26860a
Version: 4
Effective date: 2024-11-04
Source export date: 2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:15:37

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M007	openfda.application_number
brand name		Stratuscare Adult Glycerin	openfda.brand_name
generic name		GLYCERIN	openfda.generic_name
manufacturer name		Stratus Pharmaceuticals	openfda.manufacturer_name
ndc	package	58980-410-12	openfda.package_ndc
ndc	package	58980-410-25	openfda.package_ndc
ndc	package	58980-410-50	openfda.package_ndc
ndc	product	58980-410	openfda.product_ndc
ndc11	package	58980041050	derived:openfda.package_ndc
ndc11	package	58980041012	derived:openfda.package_ndc
ndc11	package	58980041025	derived:openfda.package_ndc
rxcui		104155	openfda.rxcui
spl id		14962a4b-8181-4cb7-ab2b-79877d26860a	id
spl set id		3e1935da-5c1f-4942-98dd-320fade82321	set_id
unii		PDC6A3C0OX	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. May cause rectal discomfort or burning sensation. Ask a doctor before use if you have: abdominal pain, nausea or vomiting a sudden change in bowel habits lasting more than 2 weeks. Stop use and ask a doctor: if you have rectal bleeding or fail to have a bowel movement after using a laxative. This may indicate a serious condition. Do not use laxative products for longer than 1 week unless directed by a doctor I f pregnant or breastfeeding , ask a doctor before use. Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately (1-800-222-1212).

Reported adverse events (FAERS/openFDA)#

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