FDA label 43d37bc0-2b98-660f-e063-6394a90a88c9

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
75251543-dbf9-48c3-e053-2a91aa0aaff9
SPL ID
43d37bc0-2b98-660f-e063-6394a90a88c9
Version
6
Effective date
2025-11-17
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:37:55

Warnings cross-check#

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

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings: A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES. For external use only. This product is intended to complement, not replace, standard medical treatment. Initial worsening of symptoms may occur.

warnings

Replace cap after every use. To avoid contamination: do not touch tip to any surface. Use within 30 days of opening. EXPIRATION DATE ONLY REFERS TO THE UNOPENED TUBE. The use of this container by more than one person may spread infection. Contact lens wearers: Consult a physician before use.

Reported adverse events (FAERS/openFDA)#

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