FDA.reportPublic FDA data

Zap APF

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 APF
Generic name
SODIUM FLUORIDE
Manufacturer
Crosstex International Inc.
Product type
HUMAN PRESCRIPTION DRUG
SPL set ID
537d2b3f-d7e0-49c9-aaac-680f897b63a5
SPL ID
d60ad691-00fd-da4f-e053-2a95a90a646b
Version
6
Effective date
2022-01-20
Source export date
2026-08-08
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/2026-08-08/d256baae5644161bb821f95aa5c984626cd3cdfa52f9ac98031354c0c686ab3e/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
b39f3b00ad50d2e1b32aaf429248c6081e8799b35bce715b4fccb8cfa1ac4546
Import run
20260810T161303Z
Imported at
2026-08-10 17:17:09
Harmonized routes table
Harmonized routes
DENTAL

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. Read directions carefully before using.