Boudreauxs

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: Boudreauxs
Generic name: ZINC OXIDE
Manufacturer: C.B. Fleet Company, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: f8f626c8-13ae-4b3b-ae3f-e0dc800fcb4a
SPL ID: d9877348-ea83-416f-90b9-8862ec408afe
Version: 5
Effective date: 2026-03-06
Source export date: 2026-11-06
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/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:36:16

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		Boudreauxs	openfda.brand_name
generic name		ZINC OXIDE	openfda.generic_name
manufacturer name		C.B. Fleet Company, Inc.	openfda.manufacturer_name
ndc	package	0132-0324-04	openfda.package_ndc
ndc	package	0132-0324-02	openfda.package_ndc
ndc	package	0132-0324-14	openfda.package_ndc
ndc	product	0132-0324	openfda.product_ndc
ndc11	package	00132032404	derived:openfda.package_ndc
ndc11	package	00132032414	derived:openfda.package_ndc
ndc11	package	00132032402	derived:openfda.package_ndc
rxcui		708071	openfda.rxcui
spl id		d9877348-ea83-416f-90b9-8862ec408afe	id
spl set id		f8f626c8-13ae-4b3b-ae3f-e0dc800fcb4a	set_id
unii		SOI2LOH54Z	openfda.unii

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 F o r external use only When using this product avoid contact with the eyes Stop use and ask a doctor if condition worsens or does not improve after 7 days Keep out of reach of children If swallowed, seek medical help or call Poison Control Center (1-800-222-1222) immediately.

Reported adverse events (FAERS/openFDA)#

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