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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
Advanced
Generic name
ETHYL ALCOHOL
Manufacturer
Topco Associates LLC
Product type
HUMAN OTC DRUG
SPL set ID
faaa3452-ef1e-47db-9978-5105de69d981
SPL ID
4ab94790-1ffa-d62a-e063-6294a90a1688
Version
18
Effective date
2026-02-13
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:19:04
Harmonized routes table
Harmonized routes
TOPICAL

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: hands Flammable, keep away from fire or flame.

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

Adverse event DISTRIBUTED BY TOPCO ASSOCIATES LLC ELK GROVE VILLAGE, IL 60007 ©TOPCO VIJA0223 QUESTIONS? 1-888-423-0139 topcare@topco.com WWW.TOPCAREBRAND.COM **This product is not manufactured or distributed by GOJO Industries, Inc. distributor of Purell ® Refreshing Gel Advanced Hand Sanitizer. *Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds. DSP-TN-21091 DSP-MO-20087 DSP-MO-28 SDS-MO-20068 QUALITY GUARANTEED This TopCare ® product is laboratory tested to guarantee its highest quality. Your total satisfaction is guaranteed. Scan here for more information or call 1-888-423-0139 Pat. 9,161,982

Reported adverse events (FAERS/openFDA)#

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