FDA.reportPublic FDA data

NDC 73656-035 - Optimax Purple Anticavity Fluoride

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
73656-035
Package NDCs from labels
73656-035-00
Manufacturer
WHITE GLO USA INC
Effective date
2025-09-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Optimax Purple Anticavity Fluoride - WHITE GLO USA INCWHITE GLO USA INC2025-09-02HUMAN OTC DRUG LABEL

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 118 of 223 · 4,451 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Topcare Cold and Hot MedicatedMENTHOLTopco Associates LLC8739aedd-165c-5ae0-e053-2a91aa0afcd02025-10-31WarningsExact identifier
unii: L7T10EIP3A
Honey Lemon Cough DropsMENTHOLTrader Joe's Company647dadae-f37a-8399-e053-2991aa0aedb32025-10-31WarningsExact identifier
unii: L7T10EIP3A
Dragon with Arnical Pain ReliefMENTHOLGenomma Lab USA Inc.b4cbb7b6-cb71-9721-e053-2995a90a2b2c2025-10-31WarningsExact identifier
unii: L7T10EIP3A
Classic Mint Flavor Sodium Fluoride Anticavity ToothpastSODIUM FLUORIDEHISMILE PTY LTD425a9b71-5a7f-83e6-e063-6394a90ab7032025-10-30WarningsExact identifier
application number: M021
Grape Bubblegum Flavor Sodium Fluoride Anticavity ToothpastSODIUM FLUORIDEHISMILE PTY LTD425b1a2e-7576-13a7-e063-6394a90aa8652025-10-30WarningsExact identifier
application number: M021
Family Care Muscle and JointMENTHOLUnited Exchange Corp.959af9f4-7188-91a1-e053-2995a90a46652025-10-30WarningsExact identifier
unii: L7T10EIP3A
CVS Cold and HotMENTHOLCVS Pharmacya44ca52d-fec8-0e8c-e053-2995a90a2e602025-10-30WarningsExact identifier
unii: L7T10EIP3A
TopCare Health Pain ReliefMENTHOL, CAMPHOR, AND METHYL SALICYLATETopco Associates LLCdac364ef-6dcd-3fc6-e053-2a95a90a9bb22025-10-30WarningsExact identifier
unii: L7T10EIP3A
REMEDY Calazime Skin ProtectantCALAMINE, MENTHOL, WHITE PETROLATUM, ZINC OXIDEMedline Industries, LP1295cfcc-5b61-481b-964b-f53ffd0cb58e2025-10-30WarningsExact identifier
unii: L7T10EIP3A
The Simpsons Pink Donut Flavor Sodium Fluoride Anticavity ToothpastSODIUM FLUORIDEHISMILE PTY LTD426b8efa-e691-a67d-e063-6394a90abf8d2025-10-30WarningsExact identifier
application number: M021
Muscle Rub Pain Reliever GelMENTHOL, UNSPECIFIED FORMUniversal Distribution Centre LLC18536e21-afc3-8447-e063-6394a90aabae2025-10-30WarningsExact identifier
unii: L7T10EIP3A
RELISPRAY NATURAL PAIN RELIEFMENTHOLMidas-Care Pharmaceuticals, Pvt. Ltdadc8a43c-19a1-4eb3-9820-b63f7b5e91ea2025-10-30WarningsExact identifier
unii: L7T10EIP3A
Sorbitol-MannitolSORBITOL AND MANNITOLICU Medical Inc.5b44e248-4b7b-4777-954a-921c7b3099442025-10-30Warnings, Adverse reactionsExact identifier
unii: 506T60A25R
Regular Strength AntacidCALCIUM CARBONATESAFEWAYce44254f-6e33-4cbd-a609-6a926376efaf2025-10-29WarningsExact identifier
unii: H0G9379FGK
Extra StrengthCALCIUM CARBONATEBETTER LIVING BRANDS, LLC9b311b76-1892-4b74-a07a-8b321436d4a02025-10-29WarningsExact identifier
unii: H0G9379FGK
Extra StrengthANTACID TABLETSSAFEWAYf91aa7da-8bdc-4fd2-a9de-fef21674e5152025-10-29WarningsExact identifier
unii: H0G9379FGK
Extra Strength SmoothCALCIUM CARBONATESAFEWAY4314ac58-03aa-479c-a711-4818cc3325312025-10-29WarningsExact identifier
unii: H0G9379FGK
Extra StrengthANTACID TABLETSSAFEWAY5bdb868d-016d-4175-9283-86c5b77bb26e2025-10-29WarningsExact identifier
unii: H0G9379FGK
Extra StrengthANTACID TABLETSSAFEWAY03853f03-081d-4a78-b383-66ac9754d46f2025-10-29WarningsExact identifier
unii: H0G9379FGK
Ultra StrengthCALCIUM CARBONATEBETTER LIVING BRANDS LLC3ff92c9a-987f-468e-9e18-1e3e171ede142025-10-29WarningsExact identifier
unii: H0G9379FGK

Reported adverse events (FAERS/openFDA)#

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