FDA label 73f0d4ed-2a01-c4db-e053-2a91aa0a32b9

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
12ff3cc7-d8c3-477e-bb45-e5723120c849
SPL ID
73f0d4ed-2a01-c4db-e053-2a91aa0a32b9
Version
4
Effective date
2018-08-21
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:10:51

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 insert into the vagina Do Not Use In the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites or serious burns, consult a doctor Stop Use and consult doctor; if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor

Reported adverse events (FAERS/openFDA)#

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