Zap Neutral

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: Zap Neutral
Generic name: SODIUM FLUORIDE
Manufacturer: Crosstex International Inc.
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: e1dc8865-a193-44e7-b628-3c4e5d595318
SPL ID: d5f4f5b4-2d80-6c1b-e053-2995a90ab23b
Version: 6
Effective date: 2022-01-19
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 19:56:38

Harmonized routes table
Harmonized routes
DENTAL

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Zap Neutral	openfda.brand_name
generic name		SODIUM FLUORIDE	openfda.generic_name
manufacturer name		Crosstex International Inc.	openfda.manufacturer_name
ndc	package	24794-108-16	openfda.package_ndc
ndc	product	24794-108	openfda.product_ndc
ndc11	package	24794010816	derived:openfda.package_ndc
rxcui		245593	openfda.rxcui
spl id		d5f4f5b4-2d80-6c1b-e053-2995a90ab23b	id
spl set id		e1dc8865-a193-44e7-b628-3c4e5d595318	set_id
unii		8ZYQ1474W7	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: Keep out of reach of children. Do not swallow. If product is accidentally swallowed in quantities greater than would normally occur with a treatment gel, seek medical help or contact a Poison Control Center right away. This product contains a concentrated fluoride amount and is available by prescription only. It should be used under professional supervision.

Reported adverse events (FAERS/openFDA)#

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