NDC 39892-0602-01 - MediChoice 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: 39892-0602
Requested NDC: 39892-0602-01
Package NDCs from labels: 39892-0602-1, 39892-0602-01
Manufacturer: O&M HALYARD, INC. | Owens & Minor Inc.
Effective date: 2025-10-09
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
MediChoice Fluoride Toothpaste	O&M HALYARD, INC. \| Owens & Minor Inc.	2025-10-09	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
39892-0602-1	MediChoice Fluoride	17 g in 1 TUBE	PASTE, DENTIFRICE	17		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
39892-0602	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR INC.]	5	Current NDC, Legacy NDC, 1 package rows	20231213_a87956fa-8975-4a44-9e9a-4b2191e401fe.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SODIUM MONOFLUOROPHOSPHATE	ACTIVE INGREDIENT	C810JCZ56Q	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
CALCIUM CARBONATE	INACTIVE INGREDIENT	H0G9379FGK	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
CARBOXYMETHYLCELLULOSE SODIUM	INACTIVE INGREDIENT	K679OBS311	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
POLYETHYLENE GLYCOL 400	INACTIVE INGREDIENT	B697894SGQ	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
SACCHARIN SODIUM	INACTIVE INGREDIENT	SB8ZUX40TY	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
SODIUM PYROPHOSPHATE	INACTIVE INGREDIENT	O352864B8Z	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
SODIUM SILICATE	INACTIVE INGREDIENT	IJF18F77L3	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR]	1

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 229 · 4,576 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pepcid Complete	FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE	Kenvue Brands LLC	37e6a3f6-5261-475d-a7d4-e72854088982	2025-11-05	Warnings	Exact identifier unii: H0G9379FGK
Perricone MD Cold Plasma Plus Neck and Chest Broad Spectrum SPF 25	TITANIUM DIOXIDE	THG Beauty USA LLC	23a55301-2277-6e4f-e063-6394a90af171	2025-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
WALGREENS EXTRA STRENGTH SMOOTH ANTACID	CALCIUM CARBONATE	WALGREENS CO.	9a5631e8-4287-4368-bb56-3ce22a3680d8	2025-11-04	Warnings	Exact identifier unii: H0G9379FGK
up and up extra strength antacid 750 Assorted Berry	ANTACID TABLETS	Target Corporation	46f11acf-a968-4fdd-8755-3eff0b9b67d0	2025-11-04	Warnings	Exact identifier unii: H0G9379FGK
up and up extra strength antacid 750 Assorted Berry	ANTACID TABLETS	Target Corporation	b76441ad-f701-4d0d-b9a7-18ac466faa44	2025-11-04	Warnings	Exact identifier unii: H0G9379FGK
extra strength Tropical Fruit	ANTACID	Target Corporation	b2c2fcb4-5a47-47eb-ae0e-6bc3713b161d	2025-11-04	Warnings	Exact identifier unii: H0G9379FGK
ultra strength Assorted Fruit	CALCIUM CARBONATE ANTACID	Target Corporation	a0f2ac91-c425-4e6d-8dd6-224a5b85cd2e	2025-11-04	Warnings	Exact identifier unii: H0G9379FGK
ultra strength antacid Peppermint Flavored	CALCIIUM CARBONATE	Target Corporation	55dc1614-8fc0-4f2c-abfc-b675173b4f07	2025-11-04	Warnings	Exact identifier unii: H0G9379FGK
ultra strength antacid	ANTACID	Target Corporation	2125e81b-23c6-4c5f-a6aa-829f8d3df71f	2025-11-04	Warnings	Exact identifier unii: H0G9379FGK
up and up extra strength smooth dissolving antacid Assorted berry	ANTACID TABLETS	Target Corporation	e78afe7b-a835-4fdb-9ef8-0499d1a83e6e	2025-11-04	Warnings	Exact identifier unii: H0G9379FGK
up and up extra strength smooth dissolving antacid Assorted Fruit	CALCIUM CARBONATE	Target corporation	b97558c5-d836-42ae-bfa5-0f4c6bca7e4a	2025-11-04	Warnings	Exact identifier unii: H0G9379FGK
Ultra Strength Antacid	CALCIUM CARBONATE PEPPERMINT	TARGET CORPORATION	07aa98b3-699a-bf8d-e063-6294a90a2dee	2025-11-04	Warnings	Exact identifier unii: H0G9379FGK
Extra Strength Antacid Calcium Carbonate,750 mg	CALCIUM CARBONATE	TARGET CORPORATION	07aa39bb-c409-ce4f-e063-6394a90a7069	2025-11-04	Warnings	Exact identifier unii: H0G9379FGK
Bacteriostatic Water	BACTERIOSTATIC WATER	ProPharma Distribution	42c6938e-f747-ae13-e063-6294a90a59a3	2025-11-04	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Dentisse	SODIUM FLUORIDE	Dentisse, Inc.	326b290a-9bd2-468e-e054-00144ff8d46c	2025-11-04	Warnings	Exact identifier application number: M021
Home Care Fluoride	STANNOUS FLUORIDE	Dental Technologies, Inc.	51f1d84c-809a-4c96-a117-7a8d8aa1e6b4	2025-11-04	Warnings	Exact identifier application number: M021
Home Care Fluoride	STANNOUS FLUORIDE	Dental Technologies, Inc.	c44686f8-93ee-4a8f-8481-3439d123f6d2	2025-11-04	Warnings	Exact identifier application number: M021
Home Care Fluoride	STANNOUS FLUORIDE	Dental Technologies, Inc.	16ebcb37-5703-4e10-b965-570e18434b52	2025-11-04	Warnings	Exact identifier application number: M021
Plak Smacker GREAT WHITE SHARK	SODIUM FLUORIDE	YOUNG PS ACQUISITION, LLC	ca5b91aa-f69c-4553-a2b6-acf0ca1d920e	2025-11-04	Warnings	Exact identifier application number: M021
Plak Smacker	STANNOUS FLUORIDE	Young Innovations, Inc.	e65fa41e-ce2e-53e4-e053-2995a90a24d2	2025-11-04	Warnings	Exact identifier application number: M021

Reported adverse events (FAERS/openFDA)#

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