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 119 of 223 · 4,451 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ultra StrengthCALCIUM CARBONATEBETTER LIVING BRANDS LLC35b3d9d0-b04d-4f6d-b99d-435233803d4b2025-10-29WarningsExact identifier
unii: H0G9379FGK
Ultra StrengthANTACID TABLETSSAFEWAY4c6cdd81-5145-4a1f-888f-85cf5d856c392025-10-29WarningsExact identifier
unii: H0G9379FGK
Extra Strength SmoothANTACID TABLETSSAFEWAY8ed35c3b-9878-4889-90f7-a3973cf806e02025-10-29WarningsExact identifier
unii: H0G9379FGK
GlycerinGLYCERINChain Drug Marketing Association Inc.424d91f0-ecf9-6d9b-e063-6394a90a80062025-10-29WarningsExact identifier
unii: PDC6A3C0OX
Aromalief Pain Relief Cream Orange GingerMENTHOLMarketites LLC9e8d3611-ef1b-4ac6-e053-2995a90af28a2025-10-29WarningsExact identifier
unii: L7T10EIP3A
Aromalief Calming Pain Relief Cream LavenderMENTHOLMarketites LLCb8197d52-ccfb-b008-e053-2995a90a0a532025-10-29WarningsExact identifier
unii: L7T10EIP3A
Aromalief Cozy Vanilla Pain Relief CreamMENTHOLMarketites LLC3634e55e-8c62-a782-e063-6394a90a65082025-10-29WarningsExact identifier
unii: L7T10EIP3A
WorkvieLIDOCAINE HCL, MENTHOLMarketites LLCaebaffb5-58dd-ebd5-e053-2a95a90a14ed2025-10-29WarningsExact identifier
unii: L7T10EIP3A
BENOVA PAIN AND ITCH RELIEFMENTHOL, 0.11%BENOVA RX LLC42513ee2-8b40-a9f3-e063-6394a90a93862025-10-29WarningsExact identifier
unii: L7T10EIP3A
Coralite Ultra Strength Pain ReliefCAMPHOR MENTHOLUnited Exchange Corp.44ecf959-cc07-4adc-a500-075b2ee695482025-10-29WarningsExact identifier
unii: L7T10EIP3A
Blue Raspberry Flavor Sodium Fluoride Anticavity ToothpastSODIUM FLUORIDEHISMILE PTY LTD42583b32-525f-925d-e063-6294a90af76f2025-10-29WarningsExact identifier
application number: M021
hemorrhoidalGLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUMPublix Super Markets Inc354a640c-bc7e-45c8-9df0-8b5b01767f5c2025-10-29WarningsExact identifier
unii: PDC6A3C0OX
Sterile WaterWATERICU Medical Inc.1c0bbcb7-5ed6-4ee7-b297-080d3359474e2025-10-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Publix Regular Strength Assorted FruitCALCIUM CARBONATEPUBLIX SUPER MARKETS, INCfd637431-7a08-4454-9cae-a68716d2d0fa2025-10-28WarningsExact identifier
unii: H0G9379FGK
Publix Regular Strength Peppermint FlavorCALCIUM CARBONATEPUBLIX SUPER MARKETS, INCc41b6cc2-c852-45fd-858c-c7bedc5dc8822025-10-28WarningsExact identifier
unii: H0G9379FGK
Publix Extra Strength Assorted BerryCALCIUM CARBONATEPUBLIX SUPER MARKETS, INCa270fc36-f2b2-4f56-81d4-cf165f6b5abe2025-10-28WarningsExact identifier
unii: H0G9379FGK
Extra Strength Sugar Free Orange Cream FlavorCALCIUM CARBONATEPUBLIX SUPER MARKETS, INC4dbdabc4-280d-4c9a-8c54-84afc615c8c72025-10-28WarningsExact identifier
unii: H0G9379FGK
Publix Extra Strength Tropical FruitCALCIUM CARBONATEPUBLIX SUPER MARKETS, INC28e8dd03-25cf-43db-8c4d-3aae99be9d532025-10-28WarningsExact identifier
unii: H0G9379FGK
Publix Ultra Strength Assorted FruitCALCIUM CARBONATEPUBLIX SUPER MARKETS, INC9e1c883f-016e-4c05-b27a-750d14c0f3e52025-10-28WarningsExact identifier
unii: H0G9379FGK
PERIOE KAKAO KIDS StrawberrySODIUM FLUORIDELG HOUSEHOLD & HEALTH CARE LTD.4239f8c2-a5f5-3fa6-e063-6294a90acb472025-10-28WarningsExact identifier
application number: M021

Reported adverse events (FAERS/openFDA)#

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