Rite Aid

Product NDC: 11822-5020
11-digit product format: 118225020
Labeler code: 11822
Product ID: 11822-5020_439577bb-c84a-eca0-e063-6394a90a9246
Type: HUMAN OTC DRUG
Nonproprietary name: Fluoride
Dosage form: PASTE, DENTIFRICE
Route: DENTAL
Labeler: Rite Aid
Application: M022
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2013-06-03
Marketing end: 2027-01-01
Substance: SODIUM FLUORIDE; POTASSIUM NITRATE
Active strength: .15; 5 g/100g; g/100g
NDC exclude flag: No
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Rite Aid
Brand name suffix: Extra Whitening

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM FLUORIDE	.15 g/100g
POTASSIUM NITRATE	5 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
8ZYQ1474W7	Internal UNII lookup
RU45X2JN0Z	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1038929	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
efe2c6c1-b8c6-4a52-b3c6-c9bfca450570	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11822-5020-9	Rite AidExtra Whitening	113 g in 1 TUBE	PASTE, DENTIFRICE	113		14
11822-5020-9	Rite AidExtra Whitening	1 in 1 CARTON	PASTE, DENTIFRICE	1		14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
POTASSIUM NITRATE	ACTIVE INGREDIENT	RU45X2JN0Z	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
SODIUM FLUORIDE	ACTIVE INGREDIENT	8ZYQ1474W7	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
NITRATE ION	ACTIVE MOIETY	T93E9Y2844	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
COCAMIDOPROPYL BETAINE	INACTIVE INGREDIENT	5OCF3O11KX	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
HYDRATED SILICA	INACTIVE INGREDIENT	Y6O7T4G8P9	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
POLYETHYLENE GLYCOL 400	INACTIVE INGREDIENT	B697894SGQ	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
SACCHARIN SODIUM	INACTIVE INGREDIENT	SB8ZUX40TY	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
SODIUM METHYL COCOYL TAURATE	INACTIVE INGREDIENT	JVL98CG53G	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
SODIUM TRIPOLYPHOSPHATE	INACTIVE INGREDIENT	5HK03SA80J	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1
XANTHAN GUM	INACTIVE INGREDIENT	TTV12P4NEE	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11822-5020	RITE AID EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [RITE AID]	12	Current NDC, Legacy NDC, 2 package rows	20250119_efe2c6c1-b8c6-4a52-b3c6-c9bfca450570.zip

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 7 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lemon Glycerin	GLYCERIN	Dynarex Corporation	99fc00ea-9d55-0380-e053-2995a90a2c0b	2026-03-24	Warnings	Exact identifier application number: M022
Dual-FormulaToothpaste for sensitive teeth	DUAL-FORMULA TOOTHPASTE FOR SENSITIVE TEETH	Hangzhou Namei Zhikang Technology Co., Ltd.	4d735f91-8abc-3a30-e063-6394a90a7639	2026-03-20	Warnings	Exact identifier application number: M022
SmileCare Mouth Ulcer Gel	MENTHOL	Yantai Aien Biotechnology Co., Ltd.	4d6db039-5b97-8f3f-e063-6294a90a9d85	2026-03-19	Warnings	Exact identifier application number: M022
Quala Topical Anesthetic Gel	BENZOCAINE	National Distribution & Contracting, Inc	9f91e609-8ca5-0492-e053-2a95a90a85d0	2026-03-17	Warnings	Exact identifier application number: M022
Quala Topical Anesthetic Gel	BENZOCAINE	National Distribution & Contracting, Inc	9f81ffa5-05fd-4eef-e053-2995a90aac3e	2026-03-17	Warnings	Exact identifier application number: M022
Quala Topical Anesthetic Gel	BENZOCAINE	National Distribution & Contracting, Inc	9f947366-9380-3fa9-e053-2a95a90ad49c	2026-03-17	Warnings	Exact identifier application number: M022
Quala Topical Anesthetic Gel	BENZOCAINE	National Distribution & Contracting, Inc	9f947672-4873-5546-e053-2a95a90a3c4b	2026-03-17	Warnings	Exact identifier application number: M022
Quala Topical Anesthetic Gel	BENZOCAINE	National Distribution & Contracting, Inc	9f9490c1-8bfe-3166-e053-2a95a90a7175	2026-03-17	Warnings	Exact identifier application number: M022
Quala Topical Anesthetic Gel	BENZOCAINE	National Distribution & Contracting, Inc	9f94b65d-47e3-9c6b-e053-2a95a90aa1f8	2026-03-17	Warnings	Exact identifier application number: M022
BencoCaine Topical Anesthetic	BENZOCAINE	Benco Dental	4d3e03ee-6e0f-c9ae-e063-6394a90a6f5b	2026-03-17	Warnings	Exact identifier application number: M022
HurriCaine Topical Anesthetic	BENZOCAINE	Beutlich Pharmaceuticals, LLC	043c00a6-1346-7780-e063-6294a90a3d5a	2026-03-12	Warnings	Exact identifier application number: M022
ORAL PAIN RELIEF	BENZOCAINE	Nantong Health & Beyond Hygienic Products Inc.	a5f0be98-d47e-4307-8044-304a64db774b	2026-03-11	Warnings	Exact identifier application number: M022
SENSODYNE PRONAMEL Intensive Enamel Repair Whitening	POTASSIUM NITRATE AND SODIUM FLUORIDE	Haleon US Holdings LLC	a2f9d58b-671b-4427-a971-1fceff5f2323	2026-03-09	Warnings	Exact identifier application number: M022
Sore Mouth Cleanser	HYDROGEN PEROXIDE	CVS Pharmacy, Inc.	a5dbaadf-76a8-4c48-af2d-f4455e9411f0	2026-03-09	Warnings, Adverse reactions	Exact identifier application number: M022
Hydrogen Peroxide 3 Percent	HYDROGEN PEROXIDE	Sam's West, Inc	78a3e024-73da-40b7-9d9c-099fd6ca9b9e	2026-03-03	Warnings	Exact identifier application number: M022
Sore Throat	PHENOL GLYCERIN	CVS PHARMACY, INC	9683bcfb-2f7e-48a4-aa79-500ee8df099a	2026-03-02	Warnings	Exact identifier application number: M022
Spring Gene Oil Pulling Sensitivity	POTASSIUM NITRATE	Health and Natural Beauty USA Corp	294051e3-69ec-4190-8b03-fa34988376b7	2026-02-26	Warnings	Exact identifier application number: M022
Lolleez Watermelon	PECTIN	BFY LLC	4ba8af8b-5a17-8b8c-e063-6394a90a63f3	2026-02-25	Warnings	Exact identifier application number: M022
Oral Sore Antiseptic	HYDROGEN PEROXIDE, MENTHOL	H E B	f1450866-1be4-46d9-9fe4-52d699636b4f	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M022
SIGNATURE CARE SORE THROAT CHERRY FLAVOR	PHENOL	SAFEWAY	94a2c1b9-f462-4489-b84a-825a82835d30	2026-02-23	Warnings	Exact identifier application number: M022

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
8ZYQ1474W7	SODIUM FLUORIDE	7681-49-4	SODIUM FLUORIDE
RU45X2JN0Z	POTASSIUM NITRATE	7757-79-1	POTASSIUM NITRATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1038929	potassium nitrate 5 % / sodium fluoride 0.24 % Toothpaste	PSN	efe2c6c1-b8c6-4a52-b3c6-c9bfca450570	14
1038929	potassium nitrate 0.05 MG/MG / sodium fluoride 0.0024 MG/MG Toothpaste	SCD	efe2c6c1-b8c6-4a52-b3c6-c9bfca450570	14
1038929	K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.0024 MG/MG Toothpaste	SY	efe2c6c1-b8c6-4a52-b3c6-c9bfca450570	14
1038929	Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.0024 MG/MG Toothpaste	SY	efe2c6c1-b8c6-4a52-b3c6-c9bfca450570	14
1038929	potassium nitrate 5 % / sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste	SY	efe2c6c1-b8c6-4a52-b3c6-c9bfca450570	14
1038929	potassium nitrate 5 % / sodium fluoride 0.24 % (fluoride ion 0.15 % ) Toothpaste	SY	efe2c6c1-b8c6-4a52-b3c6-c9bfca450570	14
1038929	potassium nitrate 5 % / sodium fluoride 0.24 % Toothpaste	SY	efe2c6c1-b8c6-4a52-b3c6-c9bfca450570	14

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11822-5020-9	11822502009	1 TUBE in 1 CARTON (11822-5020-9) / 113 g in 1 TUBE	1 tube	2013-06-03	2027-01-01	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
5820205 Rite Aid Max Str Sensitive Extra Whitening	Rite Aid \| Lornamead Products	2025-11-14	HUMAN OTC DRUG LABEL	14