Flotrex

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: Flotrex
Generic name: MULTIVITAMINS, SODIUM FLUORIDE 0.25 MG
Manufacturer: PureTek Corporation
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 30186998-2121-3ef2-e063-6394a90a513e
SPL ID: 39ed4312-2ed6-cb13-e063-6294a90aefc9
Version: 3
Effective date: 2025-07-14
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:33

Harmonized routes table
Harmonized routes
ORAL

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Flotrex	openfda.brand_name
generic name		MULTIVITAMINS, SODIUM FLUORIDE 0.25 MG	openfda.generic_name
manufacturer name		PureTek Corporation	openfda.manufacturer_name
ndc	package	59088-017-54	openfda.package_ndc
ndc	product	59088-017	openfda.product_ndc
ndc11	package	59088001754	derived:openfda.package_ndc
spl id		39ed4312-2ed6-cb13-e063-6294a90aefc9	id
spl set id		30186998-2121-3ef2-e063-6394a90a513e	set_id
unii		25X51I8RD4	openfda.unii
unii		TLM2976OFR	openfda.unii
unii		8ZYQ1474W7	openfda.unii
unii		935E97BOY8	openfda.unii
unii		S033EH8359	openfda.unii
unii		PQ6CK8PD0R	openfda.unii
unii		81G40H8B0T	openfda.unii
unii		P6YC3EG204	openfda.unii
unii		8K0I04919X	openfda.unii
unii		WR1WPI7EW8	openfda.unii
unii		68Y4CF58BV	openfda.unii
unii		1C6V77QF41	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

WARNING Keep out of the reach of children. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately. Caution: Do not eat or drink dairy products within one hour of fluoride administration. Should be chewed. This product, as all chewable tablets, is not recommended for children under age 4 due to risk of choking.

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

ADVERSE REACTIONS Folate: Allergic sensitization has been reported following both oral and parenteral administration of folate. Adverse reactions have been reported with specific vitamins and minerals but generally at levels substantially higher than those contained herein. However, allergic and idiosyncratic reactions are possible at lower levels.

Reported adverse events (FAERS/openFDA)#

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