Rite Aid

Product NDC: 11822-0316
11-digit product format: 118220316
Labeler code: 11822
Product ID: 11822-0316_2bedc5eb-1ab8-138c-e063-6394a90aea7c
Type: HUMAN OTC DRUG
Nonproprietary name: Benzocaine
Dosage form: GEL, DENTIFRICE
Route: ORAL
Labeler: Rite Aid
Application: M022
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2011-01-20
Marketing end: 2026-11-30
Substance: BENZOCAINE
Active strength: 20 g/100g
Pharmacologic classes: Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	11822-0316		I	Inactivated by FDA	2026-09-14
excluded package	package	11822-0316	11822-0316-4	I	Inactivated by FDA	2026-09-14
excluded package	package	11822-0316	11822-0316-9	D	Discontinued by firm	2026-09-14

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 14 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	11822-0316-9	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	11822-0316-9	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	11822-0316-9	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	11822-0316-9	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	11822-0316-9	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	11822-0316-9	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	11822-0316-9	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	11822-0316-9	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	11822-0316-3	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	11822-0316-9	D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	11822-0316-9	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	11822-0316-9	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	11822-0316-9	D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`

Additional Listing Data#

Finished product: Yes
Brand name base: Rite Aid
Brand name suffix: Maximum Strength

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZOCAINE	20 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
U3RSY48JW5	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
238910	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
5e216587-5384-464a-a4dd-07943668cabd	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
11822-0316-2	Rite AidMaximum Strength	14 g in 1 TUBE	GEL, DENTIFRICE	14	26
11822-0316-3	Rite AidMaximum Strength	9 g in 1 TUBE	GEL, DENTIFRICE	9	26
11822-0316-3	Rite AidMaximum Strength	1 in 1 BLISTER PACK	GEL, DENTIFRICE	1	26
11822-0316-9	Rite AidMaximum Strength	1 in 1 CARTON	GEL, DENTIFRICE	1	26
11822-0316-4	Rite AidMaximum Strength	1 in 1 CARTON	GEL, DENTIFRICE	1	14
11822-0316-4	Rite AidMaximum Strength	9 g in 1 TUBE	GEL, DENTIFRICE	9	14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BENZOCAINE	ACTIVE INGREDIENT	U3RSY48JW5	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	1
BENZOCAINE	ACTIVE MOIETY	U3RSY48JW5	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	1
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	1
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	1
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	1
POLYETHYLENE GLYCOL 400	INACTIVE INGREDIENT	B697894SGQ	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	1
SACCHARIN SODIUM	INACTIVE INGREDIENT	SB8ZUX40TY	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	1
SORBIC ACID	INACTIVE INGREDIENT	X045WJ989B	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11822-0316	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	24	Current NDC, Legacy NDC, 4 package rows	20250121_5e216587-5384-464a-a4dd-07943668cabd.zip
11822-0316	RITE AID MAXIMUM STRENGTH (BENZOCAINE) GEL, DENTIFRICE [RITE AID]	14	Current NDC, Legacy NDC, 2 package rows	20250119_13effad7-f363-b7fc-e063-6394a90a114c.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 1 of 42 · 825 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Opalescence Whitening Sensitivity Relief	POTASSIUM NITRATE AND SODIUM FLUORIDE	Ultradent Products, Inc.	44e94663-895b-67da-e063-6394a90a5fe6	2026-09-09	Warnings	Exact identifier application number: M022
Opalescence Sensitivity Relief Whitening	POTASSIUM NITRATE AND SODIUM FLUORIDE	Ultradent Products, Inc.	b5176a84-76a3-4ad0-a2e2-4997a12da9a5	2026-09-09	Warnings	Exact identifier application number: M022
Opal by Opalescence Sensitivity	POTASSIUM NITRATE AND SODIUM FLUORIDE	Ultradent Products, Inc.	5ffc0d14-0290-47bb-90e5-90a25a5acc28	2026-09-09	Warnings	Exact identifier application number: M022
Saline	NASAL	Raritan Pharmaceuiticals Inc	4b178e4e-a10f-4b75-8140-1f7548e203ad	2026-09-09	Warnings	Exact identifier application number: M022
SORE THROAT	PHENOL	Raritan Pharmaceuticals Inc	43ce374a-824c-4034-bf04-c351b4d8015b	2026-09-08	Warnings	Exact identifier application number: M022
Colgate Optic White Stain Fighter Sens Relief	SODIUM FLUORIDE	Colgate-Palmolive Company	6ec2fff7-df44-4302-be2d-97946c6cd66a	2026-09-08	Warnings	Exact identifier application number: M022
DRx Choice Sore Throat Menthol Flavor	PHENOL	RARITAN PHARMACEUTICALS INC	e3269b12-5c05-45a6-81f2-65d9f016c3aa	2026-09-08	Warnings	Exact identifier application number: M022
Hydrogen Peroxide	HYDROGEN PEROXIDE	AmerisourceBergen (Good Neighbor Pharmacy) 46122	0733015b-e81a-4a62-82ad-dacaf3f163cb	2026-09-02	Warnings	Exact identifier application number: M022
KROGER Saline	NASAL	KROGER COMPANY	c84b242b-f46e-4ea8-a3c1-109a47644646	2026-09-02	Warnings	Exact identifier application number: M022
Antiseptic	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	WALMART INC. (see also Equate)	ceb125d9-8c1b-498c-b0f0-f18756ede442	2026-09-01	Warnings	Exact identifier application number: M022
Orajel 4X Medicated Toothache and Gum Cream	BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	5a1c82b4-02b3-d456-e063-6294a90a16bb	2026-08-31	Warnings	Exact identifier application number: M022
Orajel 4X Medicated Toothache and Gum PM Cream	BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	5a1cdaf4-3388-280c-e063-6294a90ac70f	2026-08-31	Warnings	Exact identifier application number: M022
MUCINEX INSTASOOTHE SORE THROAT PLUS SOOTHING COMFORT	HEXYLRESORCINOL	Reckitt Benckiser LLC	91cd2964-5d83-4e40-bc18-e3e5462f454a	2026-08-31	Warnings	Exact identifier application number: M022
MUCINEX INSTASOOTHE SORE THROAT PLUS PAIN RELIEF	HEXYLRESORCINOL	Reckitt Benckiser LLC	4c150222-06ea-4fcf-967f-84e19846bd66	2026-08-31	Warnings	Exact identifier application number: M022
Orajel 4X Medicated Toothache and Gum	BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE	Church & Dwight Co., Inc.	5a1b4133-0eac-2f8f-e063-6394a90af8f6	2026-08-28	Warnings	Exact identifier application number: M022
LUDENS SUGAR FREE WILD CHERRY THROAT	PECTIN	Prestige Brands Holdings, Inc.	274fc80c-e5b2-41c7-a119-287d6e8a2258	2026-08-28	Warnings	Exact identifier application number: M022
Medline Peroxi Fresh Mouthwash	HYDROGEN PEROXIDE	Medline Industries, LP	ec7a9240-6c66-4471-b8b6-776e08a14fbc	2026-08-27	Warnings	Exact identifier application number: M022
Saline	SALINE NASAL SPRAY	Dynarex Corporation	3247ae7d-554f-baab-e063-6294a90aa3ec	2026-08-25	Warnings	Exact identifier application number: M022
Tumeez Organic Apple	CALCIUM CARBONATE	BFY LLC	f561685a-5260-59c6-e053-2a95a90ae206	2026-08-25	Warnings	Exact identifier application number: M022
Ludens Watermelon Throat Drops	PECTIN	Prestige Brands Holdings, Inc.	adfb248a-96bb-4742-9df6-c47edccdd671	2026-08-20	Warnings	Exact identifier application number: M022

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
U3RSY48JW5	BENZOCAINE	94-09-7	BENZOCAINE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
238910	benzocaine 20 % Oral Gel	PSN	5e216587-5384-464a-a4dd-07943668cabd	26
238910	benzocaine 0.2 MG/MG Oral Gel	SCD	5e216587-5384-464a-a4dd-07943668cabd	26
238910	benzocaine 20 % (180-220 MG per 1 GM) Oral Gel	SY	5e216587-5384-464a-a4dd-07943668cabd	26
238910	benzocaine 20 % Oral Gel	PSN	13effad7-f363-b7fc-e063-6394a90a114c	14
238910	benzocaine 0.2 MG/MG Oral Gel	SCD	13effad7-f363-b7fc-e063-6394a90a114c	14
238910	benzocaine 20 % (180-220 MG per 1 GM) Oral Gel	SY	13effad7-f363-b7fc-e063-6394a90a114c	14

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11822-0316-2	11822031602	14 g in 1 TUBE	14 g					Historical
11822-0316-3	11822031603	1 TUBE in 1 BLISTER PACK (11822-0316-3) / 9 g in 1 TUBE	1 tube	2019-03-03	2026-11-30	No	No	Current
11822-0316-4	11822031604	1 TUBE in 1 CARTON (11822-0316-4) / 9 g in 1 TUBE	1 tube	2024-03-14		No	No	Historical
11822-0316-9	11822031609	1 in 1 CARTON						Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
5820366 Rite Aid Max Str Oral Pain Relief Gel	Rite Aid \| Lornamead Products	2025-11-21	HUMAN OTC DRUG LABEL	26
5820630 Rite Aid Max Str Oral Pain Relief Gel (8015316)	Rite Aid \| Lornamead Inc.	2025-01-17	HUMAN OTC DRUG LABEL	14