Home DailyMed 5c3abf2c-c65b-cd4e-e063-6294a90a4e91 Crest Plus Scope plus Whitening Ultra Mint Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer The Procter & Gamble Manufacturing Company | Ryder Integrated Logistics, Inc
Effective date 2026-09-24
Label type HUMAN OTC DRUG LABEL
Version 3
Source daily-update
Hydrated at 2026-09-26 01:01:48 Label at a glance# Product Crest Plus Scope plus Whitening Ultra Mint
Active ingredient SODIUM FLUORIDE
Label structure 10 sections
Dosage and administration adults and children 2 yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist do not swallow to minimize swallowing use a pea-sized amount in children under 6 supervise children's brushing until good habits are established children under 2 yrs.: ask a dentist
Product Linked Resources# Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 21 matching rows.
Crest Plus Scope plus Whitening Ultra Mint Sodium Fluoride FLUORIDE ION SUCRALOSE BLUE 1 POLYSORBATE 80 SODIUM SACCHARIN CETYLPYRIDINIUM CHLORIDE TITANIUM DIOXIDE SODIUM HYDROXIDE XANTHAN GUM SORBITOL WATER POLOXAMER 407 HYDRATED SILICA SODIUM LAURYL SULFATE ALCOHOL COCAMIDOPROPYL BETAINE GLYCERIN YELLOW 5 DISODIUM PYROPHOSPHATE Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 19 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 38 of 39 · 768 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join KOLORZ NEUTRAL FLUORIDE FOAM TRIPLE MINT SODIUM FLUORIDE DMG AMERICA, LLC b83c62be-8e9d-4fa2-aa10-d34c88bf2387 2021-10-01 Warnings Name fallback generic name: SODIUM FLUORIDE KOLORZ SIXTY SECOND FLUORIDE FOAM TRIPLE MINT SODIUM FLUORIDE DMG AMERICA, LLC 427f25e6-e50a-407a-a6f0-512123e381e4 2021-10-01 Warnings Name fallback generic name: SODIUM FLUORIDE Wentworth Alcohol Free SODIUM FLUORIDE Sheffield Pharmaceuticals LLC 5ed816ef-20bc-49ac-9202-8fac1edac579 2021-03-23 Warnings, Adverse reactions Name fallback generic name: SODIUM FLUORIDE Sodium Fluoride 5000 ppm Dry Mouth SODIUM FLUORIDE Sheffield Pharmaceuticals LLC cbc67f03-55c4-4781-ba37-87c737b60282 2021-03-02 Warnings, Adverse reactions Name fallback generic name: SODIUM FLUORIDE Ionite APF SODIUM FLUORIDE Dharma Research, Inc. ab9b07ad-f6b2-4289-bec4-fec58270dc97 2021-02-20 Warnings Name fallback generic name: SODIUM FLUORIDE Avant SODIUM FLUORIDE Dharma Research, Inc. 4749dce1-c0b9-4737-8a30-85cd58aba21b 2021-01-25 Warnings, Adverse reactions Name fallback generic name: SODIUM FLUORIDE Avant SODIUM FLUORIDE Dharma Research, Inc. 184bbe52-3909-45f6-b4d0-fe7849fabc1c 2021-01-25 Warnings, Adverse reactions Name fallback generic name: SODIUM FLUORIDE Ionite APF Neutral SODIUM FLUORIDE Dharma Research, inc. ad7a660b-274c-417e-bdf3-1d5addf06ad1 2020-11-18 Warnings Name fallback generic name: SODIUM FLUORIDE Ionite APF SODIUM FLUORIDE Dharma Research, inc. 8ff1b377-0535-4548-a109-f9f1a43b85b7 2020-11-16 Warnings Name fallback generic name: SODIUM FLUORIDE Ionite APF SODIUM FLUORIDE Dharma Research, inc. e6c31330-43e0-4d32-af54-ff852af39cab 2020-11-16 Warnings Name fallback generic name: SODIUM FLUORIDE Ionite APF SODIUM FLUORIDE Dharma Research, inc. bc9664df-c4eb-4d29-b1c0-4d4dff6a75e4 2020-11-16 Warnings Name fallback generic name: SODIUM FLUORIDE Ionite APF SODIUM FLUORIDE Dharma Research, inc. b8b7f9b8-ff11-4a76-ab36-7822c15e1892 2020-11-16 Warnings Name fallback generic name: SODIUM FLUORIDE Ionite APF SODIUM FLUORIDE Dharma Research, inc. e1797adf-4665-4322-a3aa-dd2da9dcd3a8 2020-11-16 Warnings Name fallback generic name: SODIUM FLUORIDE Ionite APF SODIUM FLUORIDE Dharma Research, inc. ce34c159-34cd-47c7-937f-743b3309742b 2020-11-16 Warnings Name fallback generic name: SODIUM FLUORIDE Ionite APF SODIUM FLUORIDE Dharma Research, inc. 503ca71a-f50c-4406-b925-5b6ac36a9212 2020-11-15 Warnings Name fallback generic name: SODIUM FLUORIDE Ionite R SODIUM FLUORIDE Dharma Research, Inc. 1009afc7-6e9d-417f-a702-f8a941e08484 2020-11-06 Warnings, Adverse reactions Name fallback generic name: SODIUM FLUORIDE Ionite R SODIUM FLUORIDE Dharma Research, Inc. 0e7b3eb3-3a9e-4a51-b2b5-9f36876fc8a5 2020-11-06 Warnings, Adverse reactions Name fallback generic name: SODIUM FLUORIDE Ionite APF Foam SODIUM FLUORIDE Dharma Research, inc. d22afac7-45d6-467e-951a-e7c241b9180d 2020-10-27 Warnings Name fallback generic name: SODIUM FLUORIDE Ionite APF Foam SODIUM FLUORIDE Dharma Research, inc. 4828b482-486f-4105-bed0-3fe2ddbbddb1 2020-10-27 Warnings Name fallback generic name: SODIUM FLUORIDE Ionite APF Foam SODIUM FLUORIDE Dharma Research, Inc. 8987b447-3fa3-4f52-aecc-80e44c981aaa 2020-10-27 Warnings Name fallback generic name: SODIUM FLUORIDE
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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