FDA label 0a15627b-60c0-de5a-e063-6394a90abd4c

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: f3e1fc6d-20f6-4115-e053-2995a90ad5ca
SPL ID: 0a15627b-60c0-de5a-e063-6394a90abd4c
Version: 2
Effective date: 2023-11-13
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 05:52:37

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		0a15627b-60c0-de5a-e063-6394a90abd4c	id
spl set id		f3e1fc6d-20f6-4115-e053-2995a90ad5ca	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

Warnings For external use only

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

Stomach bleeding warning This product contains a NSAID, which may cause stomach bleeding. The chance is smaill but higher if you · are aged 60 or older · have had stomach ulcers or bleeding problems · take other drugs containing an NSAID (Aspirin, Ibuprofen, Naproxen, or others) · take a blood thinning (anticoagulant) or steroidal drug · have three or more alcoholic drinks every day while using this product · take more or for a longer time than directed.

Reported adverse events (FAERS/openFDA)#

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