FDA label 101b73d7-7130-311b-e063-6294a90afd67

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
6dd75810-da93-28aa-e053-2a91aa0a0dab
SPL ID
101b73d7-7130-311b-e063-6294a90afd67
Version
7
Effective date
2024-01-29
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 06:19:08

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 Avoid contact with eyes When using this product do not place into the rectum with fingers or any device or applicator keep out of reach of children Stop use and ask a doctor if condition worsens or does not improve within 7 days bleeding occurs an allergic reaction develops with symptoms such as redness, irritation, or pain Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not exceed the recommended daily dosage unless directed by a doctor. Certain persons can develop allergic reactions to ingredients in this product. If the symptoms being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase, discontinue use and consult a doctor.

Reported adverse events (FAERS/openFDA)#

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