BIOCENCE

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
BIOCENCE
Generic name
EUCALYPTOL, THYMOL
Manufacturer
Bio-Germ Protection LLC
Product type
HUMAN OTC DRUG
SPL set ID
9e8165f4-17b5-4d49-87ea-4926b687a235
SPL ID
45a090f6-0dfe-ae7b-e063-6394a90a9379
Version
7
Effective date
2025-12-10
Source export date
2026-11-06
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:42:36
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. DO NOT USE IN EYES OR APPLY OVER LARGE AREAS OF THE BODY. IN CASE OF DEEP OR PUNCTURE WOUNDS, ANIMAL BITES, OR SERIOUS BURNS, CONSULT A PHYSICIAN. STOP OR CONSULT A PHYSICIAN IF CONDITIONS PERSIST OR GET WORSE. DO NOT USE LONGER THAN ONE WEEK UNLESS DIRECTED BY A PHYSICIAN.

Reported adverse events (FAERS/openFDA)#

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