MIPaste Plus Strawberry

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: MIPaste Plus Strawberry
Generic name: SODIUM FLUORIDE
Manufacturer: GC America Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 1b68bd67-65d3-4c64-e054-00144ff8d46c
SPL ID: 51a07861-c024-d263-e063-6294a90ab72e
Version: 10
Effective date: 2026-05-12
Source export date: 2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:14

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 · 33 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M021	openfda.application_number
brand name		MIPaste Plus Strawberry	openfda.brand_name
generic name		SODIUM FLUORIDE	openfda.generic_name
manufacturer name		GC America Inc.	openfda.manufacturer_name
ndc	package	61596-888-41	openfda.package_ndc
ndc	package	61596-882-41	openfda.package_ndc
ndc	package	61596-884-40	openfda.package_ndc
ndc	package	61596-986-40	openfda.package_ndc
ndc	package	61596-888-40	openfda.package_ndc
ndc	package	61596-882-40	openfda.package_ndc
ndc	package	61596-884-41	openfda.package_ndc
ndc	package	61596-880-40	openfda.package_ndc
ndc	package	61596-986-41	openfda.package_ndc
ndc	package	61596-880-41	openfda.package_ndc
ndc	product	61596-882	openfda.product_ndc
ndc	product	61596-888	openfda.product_ndc
ndc	product	61596-986	openfda.product_ndc
ndc	product	61596-880	openfda.product_ndc
ndc	product	61596-884	openfda.product_ndc
ndc11	package	61596088240	derived:openfda.package_ndc
ndc11	package	61596098641	derived:openfda.package_ndc
ndc11	package	61596088840	derived:openfda.package_ndc
ndc11	package	61596088241	derived:openfda.package_ndc
ndc11	package	61596088040	derived:openfda.package_ndc
ndc11	package	61596088041	derived:openfda.package_ndc
ndc11	package	61596088440	derived:openfda.package_ndc
ndc11	package	61596088441	derived:openfda.package_ndc
ndc11	package	61596098640	derived:openfda.package_ndc
ndc11	package	61596088841	derived:openfda.package_ndc
rxcui		1235783	openfda.rxcui
spl id		51a07861-c024-d263-e063-6294a90ab72e	id
spl set id		1b68bd67-65d3-4c64-e054-00144ff8d46c	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 Do not use on patients with a milk protein or hydroxybenzoates allergy. In case of allergic reaction, stop use, rinse mouth with water and seek medical advice. If you accidentally swallow more than used for brushing, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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