BD E-Z Scrub 107

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
BD E-Z Scrub 107
Generic name
CHLORHEXIDINE GLUCONATE
Manufacturer
Becton Dickinson and Company
Product type
HUMAN OTC DRUG
SPL set ID
7c173111-11de-4585-af06-b329fe029036
SPL ID
4576e2fe-9f2a-8933-e063-6394a90a65cb
Version
9
Effective date
2025-12-08
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 05:54:46
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Do not use as a preoperative skin preparation of the face or head in eyes, ears and mouth if you have a sensitivity to chlorhexidine gluconate or its components. When using this product avoid contact with meninges chlorhexidine gluconate has been reported to cause deafness when instilled in the middle ear through perforated ear drums chlorhexidine gluconate solution has been reported to cause serious and permanent eye injury when it has been permitted to enter and remain in the eye during surgical procedures if chlorhexidine gluconate solution should contact these areas, rinse out promptly and thoroughly with water. Stop use and ask a doctor if adverse reactions occur. Irritation, sensitization and generalized allergic reactions have been reported with chlorhexidine-containing products, especially in the genital areas. Keep out of reach of children. If swallowed, gets in eye or ear, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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