NDC 11291-243-01 - Dr Tichenors With Extra Whitening and Tartar Control

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: 11291-243
Requested NDC: 11291-243-01
Package NDCs from labels: 11291-243-01, 11291-243-02
Manufacturer: Dr. G. H. Tichenor's Antiseptic Company | Lornamead Products
Effective date: 2025-11-12
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Sodium Fluoride - Dr. G. H. Tichenor's Antiseptic Company \| Lornamead Products	Dr. G. H. Tichenor's Antiseptic Company \| Lornamead Products	2025-11-12	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11291-243-01	Dr Tichenors With Extra Whitening and Tartar Control	181 g in 1 TUBE	PASTE, DENTIFRICE	181		8
11291-243-02	Dr Tichenors With Extra Whitening and Tartar Control	1 in 1 CARTON	PASTE, DENTIFRICE	1		8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11291-243	DR TICHENORS WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE, DENTIFRICE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	7	Current NDC, Legacy NDC, 2 package rows	20250112_bce596e8-07eb-4e56-9007-9d283e14372d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SODIUM FLUORIDE	ACTIVE INGREDIENT	8ZYQ1474W7	DR TICHENORS TOOTHPASTE WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	1
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	DR TICHENORS TOOTHPASTE WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	1
CARBOXYMETHYLCELLULOSE SODIUM	INACTIVE INGREDIENT	K679OBS311	DR TICHENORS TOOTHPASTE WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	DR TICHENORS TOOTHPASTE WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	1
HYDRATED SILICA	INACTIVE INGREDIENT	Y6O7T4G8P9	DR TICHENORS TOOTHPASTE WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	1
PAPAIN	INACTIVE INGREDIENT	A236A06Y32	DR TICHENORS TOOTHPASTE WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	1
POTASSIUM PYROPHOSPHATE	INACTIVE INGREDIENT	B9W4019H5G	DR TICHENORS TOOTHPASTE WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	1
SACCHARIN SODIUM ANHYDROUS	INACTIVE INGREDIENT	I4807BK602	DR TICHENORS TOOTHPASTE WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	1
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	DR TICHENORS TOOTHPASTE WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	DR TICHENORS TOOTHPASTE WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	DR TICHENORS TOOTHPASTE WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	DR TICHENORS TOOTHPASTE WITH EXTRA WHITENING AND TARTAR CONTROL (SODIUM FLUORIDE) PASTE [DR. G. H. TICHENOR'S ANTISEPTIC COMPANY]	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 37 of 195 · 3,892 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SEYTU Body Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	Omnilife USA, Inc.	c411e9a6-b2ea-446b-a886-b92c61736e6c	2026-02-05	Warnings	Exact identifier unii: 15FIX9V2JP
SEYTU Facial Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	Omnilife USA, Inc.	96fd37fb-c3ff-413f-b2c8-50754f320ecc	2026-02-05	Warnings	Exact identifier unii: 15FIX9V2JP
Crest Pro-Health Sensitivity Whitening Plus Scope	SODIUM FLUORIDE AND POTASSIUM NITRATE	The Procter & Gamble Manufacturing Company	463b7820-a5ce-f8b5-e063-6394a90aa018	2026-02-05	Warnings	Exact identifier application number: M021 unii: 8ZYQ1474W7
Anticavity	SODIUM FLUORIDE	Publix Super Markets, Inc.	14494238-872b-49e2-8bf7-df3844a0a6c8	2026-02-05	Warnings, Adverse reactions	Exact identifier application number: M021 unii: 8ZYQ1474W7
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Bamboo	OCTINOXATE, TITANIUM DIOXIDE	BCM Cosmetique SAS	ebfe03e7-614f-44b1-b1f1-78edc7e274cc	2026-02-05	Warnings	Exact identifier unii: 15FIX9V2JP
HAPEE EXPLOSIVE MENTHOL RED 150	SODIUM MONOFLUOROPHOSPHATE	LAMOIYAN CORPORATION	14c14694-6149-40a8-aff2-660d39f7e0c1	2026-02-05	Warnings	Exact identifier application number: M021 unii: 8ZYQ1474W7
SHISEIDO URBAN ENVIRONMENT oil-free MINERAL SUNSCREEN SPF 42	TITANIUM DIOXIDE AND ZINC OXIDE	SHISEIDO AMERICAS CORPORATION	86630e82-f249-4866-82dd-3e21feb266c4	2026-02-04	Warnings	Exact identifier unii: 15FIX9V2JP
Anticavity Fluoride Rinse	SODIUM FLUORIDE	HARRIS TEETER	f759e9e4-6de2-4b80-903b-e67c06e36295	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M021 unii: 8ZYQ1474W7
Oral Antivavity	SODIUM FLUORIDE	HARRIS TEETER	571f7628-fd59-462f-96dd-67aeaa98cff1	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M021 unii: 8ZYQ1474W7
Anticavity Fluoride Rinse	SODIUM FLUORIDE	Lidl US, LLC	c47475aa-3125-410f-aa31-0add6e4ce125	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M021 unii: 8ZYQ1474W7
Crest 3D White Brilliance Pro Ultra White	SODIUM MONOFLUOROPHOSPHATE	The Procter & Gamble Manufacturing Company	f4c02924-95ee-09d2-e053-2995a90a8121	2026-02-03		Exact identifier application number: M021
Crest 3D White Stain Eraser Icy Clean Mint	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	f5d97011-7be3-3b1c-e053-2a95a90ade86	2026-02-03		Exact identifier application number: M021 rxcui: 891775 unii: 8ZYQ1474W7
Anticavity	SODIUM FLUORIDE	Demoulas Super Markets, Inc.	c28c3475-efbb-4099-83ab-ab91bac9dfc3	2026-02-03	Warnings, Adverse reactions	Exact identifier application number: M021 unii: 8ZYQ1474W7
Anticavity Fluoride Rinse	SODIUM FLUORIDE	Demoulas Super Markets, Inc	65abfb4d-3a1e-42df-b343-f270ce60a3bf	2026-02-03	Warnings, Adverse reactions	Exact identifier application number: M021 unii: 8ZYQ1474W7
Crest Cavity Protection Cool Mint Gel	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	102e4d9c-0fae-d48a-e063-6294a90aac94	2026-02-03	Warnings	Exact identifier application number: M021 rxcui: 891775 unii: 8ZYQ1474W7
Crest Plus Tartar Protection	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	08767b0f-ed6e-8d32-e063-6294a90a10cd	2026-02-03	Warnings	Exact identifier application number: M021 rxcui: 891775 unii: 8ZYQ1474W7
Crest Braces Care Anticavity Fluoride Rinse	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	d8398cfd-9af6-690d-e053-2995a90a9b7c	2026-02-03	Warnings	Exact identifier application number: M021 unii: 8ZYQ1474W7
AutoBrush bubblegum	SODIUM FLUORIDE	Lander Enterprises, LLC	2e85d6f7-2df8-4eb9-bc97-d7b7af7fb460	2026-02-03	Warnings	Exact identifier application number: M021 rxcui: 891775 unii: 8ZYQ1474W7
AutoBrush Mint	SODIUM FLUORIDE	Lander Enterprises, LLC	d859d02d-a036-4d90-bed4-9a5c31e9e1ef	2026-02-03	Warnings	Exact identifier application number: M021 rxcui: 891775 unii: 8ZYQ1474W7
Glowing White	SODIUM FLUORIDE	Demoulas Super Markets, Inc	32faf47d-b64f-4454-9f14-51503504c6b5	2026-02-03	Warnings, Adverse reactions	Exact identifier application number: M021 unii: 8ZYQ1474W7

Reported adverse events (FAERS/openFDA)#

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