ADVANCED WHITENING ANTI CAVITY FLUORIDE

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
ADVANCED WHITENING ANTI CAVITY FLUORIDE
Generic name
SODIUM MONOFLUOROPHOSPHATE
Manufacturer
Universal Distribution Center LLC
Product type
HUMAN OTC DRUG
SPL set ID
8ea8a8d9-b7e4-468f-9a09-4ec634cbd80e
SPL ID
ede5654c-864e-44c6-904b-ca2ac4532096
Version
2
Effective date
2023-11-16
Source export date
2026-11-06
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/bbdc0a42bf44145a63c3752991067bece7e2a518be6cc14943d33c4987faa012/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:12:22
Harmonized routes table
Harmonized routes
DENTAL

Warnings cross-check#

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warnings

Warning

Reported adverse events (FAERS/openFDA)#

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