Tiger Supply Inc 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: Tiger Supply Inc APF
Generic name: SODIUM FLUORIDE
Manufacturer: Tiger Supply Inc
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 7da82945-3186-40b2-b67e-642bdfa9578a
SPL ID: d608a58b-315f-8753-e053-2995a90ab4c5
Version: 3
Effective date: 2022-01-20
Source export date: 2026-10-30
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/2026-10-30/772d0e4623a189b47f3ab71d7d51f9b3c89c5526f4cf3d218e1c921bb964b80c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:28:24

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		Tiger Supply Inc APF	openfda.brand_name
generic name		SODIUM FLUORIDE	openfda.generic_name
manufacturer name		Tiger Supply Inc	openfda.manufacturer_name
ndc	package	69484-050-15	openfda.package_ndc
ndc	product	69484-050	openfda.product_ndc
ndc11	package	69484005015	derived:openfda.package_ndc
rxcui		245593	openfda.rxcui
spl id		d608a58b-315f-8753-e053-2995a90ab4c5	id
spl set id		7da82945-3186-40b2-b67e-642bdfa9578a	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. Read directions carefully before using.

Reported adverse events (FAERS/openFDA)#

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