Water-Jel 3-in-1 Antibiotic

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: Water-Jel 3-in-1 Antibiotic
Generic name: BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE
Manufacturer: Water-Jel Technologies
Product type: HUMAN OTC DRUG
SPL set ID: d5fcaffd-af38-4285-a79c-6df7424c76fa
SPL ID: 5e332a38-e153-d2c4-e053-2a91aa0abb49
Version: 15
Effective date: 2017-11-16
Source export date: 2026-10-27
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:58:51

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 · 22 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		part333B	openfda.application_number
brand name		Water-Jel 3-in-1 Antibiotic	openfda.brand_name
generic name		BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE	openfda.generic_name
manufacturer name		Water-Jel Technologies	openfda.manufacturer_name
ndc	package	59898-740-34	openfda.package_ndc
ndc	package	59898-740-01	openfda.package_ndc
ndc	package	59898-740-38	openfda.package_ndc
ndc	package	59898-740-36	openfda.package_ndc
ndc	package	59898-740-03	openfda.package_ndc
ndc	package	59898-740-02	openfda.package_ndc
ndc	product	59898-740	openfda.product_ndc
ndc11	package	59898074036	derived:openfda.package_ndc
ndc11	package	59898074034	derived:openfda.package_ndc
ndc11	package	59898074002	derived:openfda.package_ndc
ndc11	package	59898074001	derived:openfda.package_ndc
ndc11	package	59898074038	derived:openfda.package_ndc
ndc11	package	59898074003	derived:openfda.package_ndc
spl id		5e332a38-e153-d2c4-e053-2a91aa0abb49	id
spl set id		d5fcaffd-af38-4285-a79c-6df7424c76fa	set_id
unii		89Y4M234ES	openfda.unii
unii		057Y626693	openfda.unii
unii		19371312D4	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 For external use only Do not use in the eyes or over large areas of the body if you are allergic to any of the ingredients longer than 1 week unless directed by a doctor Ask a doctor before use if you have a deep or puncture wounds, animal bites, or serious burns Stop use and ask a doctor if Keep out of the reach of children If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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