Rite Aid

Product NDC: 11822-0345
11-digit product format: 118220345
Labeler code: 11822
Product ID: 11822-0345_437fc201-e0df-b2d6-e063-6394a90a9d24
Type: HUMAN OTC DRUG
Nonproprietary name: Benzocaine
Dosage form: LIQUID
Route: ORAL
Labeler: Rite Aid
Application: M022
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2015-01-01
Marketing end: 2027-01-01
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
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: 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
308657	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
340ccdab-0a02-454c-8d44-ced5667276ab	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11822-0345-1	Rite AidMaximum Strength	14.7 g in 1 BOTTLE	LIQUID	14.7		15
11822-0345-7	Rite AidMaximum Strength	1 in 1 CARTON	LIQUID	1		15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BENZOCAINE	ACTIVE INGREDIENT	U3RSY48JW5	RITE AID MAXIMUM STRENGTH (BENZOCAINE) LIQUID [RITE AID]	1
BENZOCAINE	ACTIVE MOIETY	U3RSY48JW5	RITE AID MAXIMUM STRENGTH (BENZOCAINE) LIQUID [RITE AID]	1
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	RITE AID MAXIMUM STRENGTH (BENZOCAINE) LIQUID [RITE AID]	1
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	RITE AID MAXIMUM STRENGTH (BENZOCAINE) LIQUID [RITE AID]	1
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	RITE AID MAXIMUM STRENGTH (BENZOCAINE) LIQUID [RITE AID]	1
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	RITE AID MAXIMUM STRENGTH (BENZOCAINE) LIQUID [RITE AID]	1
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	RITE AID MAXIMUM STRENGTH (BENZOCAINE) LIQUID [RITE AID]	1
POLYETHYLENE GLYCOL 400	INACTIVE INGREDIENT	B697894SGQ	RITE AID MAXIMUM STRENGTH (BENZOCAINE) LIQUID [RITE AID]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	RITE AID MAXIMUM STRENGTH (BENZOCAINE) LIQUID [RITE AID]	1
SACCHARIN SODIUM	INACTIVE INGREDIENT	SB8ZUX40TY	RITE AID MAXIMUM STRENGTH (BENZOCAINE) LIQUID [RITE AID]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11822-0345	RITE AID MAXIMUM STRENGTH (BENZOCAINE) LIQUID [RITE AID]	13	Current NDC, Legacy NDC, 2 package rows	20250119_340ccdab-0a02-454c-8d44-ced5667276ab.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 36 of 40 · 782 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Attitude Adult Fluoride-free - Sensitive - Spearmint	POTASSIUM NITRATE	9055-7588 Qubec Inc. DBA Attitude	46d5c908-f0e3-444c-9d96-461feef39137	2024-05-14	Warnings	Exact identifier application number: M022
sensodyne	POTASSIUM NITRATE AND SODIUM FLUORIDE	Haleon US Holdings LLC	16225f06-1d40-416a-aaec-7890e398fe4b	2024-05-13	Warnings	Exact identifier application number: M022
Sore Throat Cherry	PHENOL	QUALITY CHOICE (Chain Drug Marketing Association)	9162ae27-ddbb-4336-9655-487995919de4	2024-05-01	Warnings	Exact identifier application number: M022
BIO SPECTRA ATTITUDE	SODIUM FLUORIDE AND POTASSIUM NITRATE	9055-7588 Quebec Inc. DBA Attitude	42b79ec5-f37f-4dc9-9631-c8b1c153fe88	2024-04-26	Warnings	Exact identifier application number: M022
Quality Choice Oral Pain Relief	BENZOCAINE 20%, BENZALKONIUM CHLORIDE 1%	Quality Choice (CHAIN DRUG MARKETING ASSOCIATION)	162702b4-4bf7-8868-e063-6294a90a5921	2024-04-15	Warnings	Exact identifier application number: M022
Gelato Topical Anesthetic	BENZOCAINE	Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc	9991de96-99a1-42f0-9ddd-e530ca9ceab1	2024-04-11	Warnings	Exact identifier application number: M022
Aquafresh Extreme Clean Pure Breath Action	SODIUM FLUORIDE	Haleon US Holdings LLC	462eb309-deca-4464-b13a-7ae314e53ede	2024-04-08	Warnings	Exact identifier application number: M022
Sore Throat Cherry	PHENOL	Family Dollar (FAMILY WELLNESS)	7806fac7-736e-44b0-baa2-42feb7237417	2024-03-27	Warnings	Exact identifier application number: M022
Sucrets	DYCLONINE HCL, MENTHOL, AND PECTIN	Insight Pharmaceuticals LLC	2a2839ea-11d3-4390-930d-0da912a9c6f5	2024-03-20	Warnings	Exact identifier application number: M022
Sucrets Sore Throat Wild Cherry	DYCLONINE HYDROCHLORIDE	Insight Pharmaceuticals LLC	da4967c7-ee18-42e7-8c97-8919f3bb1b7d	2024-03-20	Warnings	Exact identifier application number: M022
NATEAN Clean plus Sensitivity Relief	POTASSIUM NITRATE, SODIUM FLUORIDE	Haleon US Holdings LLC	cea6f992-8a44-4eb8-baea-97b7b181b227	2024-03-19	Warnings	Exact identifier application number: M022
NATEAN Clean and Whiten	SODIUM FLUORIDE	Haleon US Holdings LLC	71b95962-2693-49f5-94d2-f2a035b5e0c8	2024-03-19	Warnings	Exact identifier application number: M022
SENSODYNE Sensitivity and Gum Mint	STANNOUS FLUORIDE	Haleon US Holdings LLC	ed093acd-255c-40ff-a010-d276f5844453	2024-03-07	Warnings	Exact identifier application number: M022
SENSODYNE Sensitivity Gum and Enamel Mint	STANNOUS FLUORIDE	Haleon US Holdings LLC	d4e9e5cf-d058-4c3f-ab5e-0b5a20a012e2	2024-03-07	Warnings	Exact identifier application number: M022
Sensodyne True white	POTASSIUM NITRATE AND SODIUM FLUORIDE	Haleon US Holdings LLC	671f8f45-389c-4375-be43-f5500ee21a0e	2024-03-07	Warnings	Exact identifier application number: M022
Sensodyne Pronamel Strong and Bright Enamel Mint	POTASSIUM NITRATE AND SODIUM FLUORIDE	Haleon US Holdings LLC	be1ae382-0e01-4db8-90d7-fdadec2ff861	2024-03-06	Warnings	Exact identifier application number: M022
SENSODYNE Rapid Relief	STANNOUS FLUORIDE	Haleon US Holdings LLC	f9589e7c-c5ca-4465-8d37-47ad6c69249f	2024-03-06	Warnings	Exact identifier application number: M022
SENSODYNE Repair and Protect Extra Fresh	STANNOUS FLUORIDE	Haleon US Holdings LLC	34260c69-d829-46c0-b12a-5136ee073ba1	2024-03-06	Warnings	Exact identifier application number: M022
AQUAFRESH SENSITIVE MAXIMUM STRENGTH	POTASSIUM NITRATE AND SODIUM FLUORIDE	Haleon US Holdings LLC	76adbccb-0812-4407-a6fc-a57e6f144fbb	2024-03-05	Warnings	Exact identifier application number: M022
SENSODYNE Advanced Whitening	POTASSIUM NITRATE	Haleon US Holdings LLC	a06e2549-3c4e-4818-b53e-1dea6828219f	2024-03-04	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
308657	benzocaine 20 % Mucous Membrane Topical Solution	PSN	340ccdab-0a02-454c-8d44-ced5667276ab	15
308657	benzocaine 200 MG/ML Mucous Membrane Topical Solution	SCD	340ccdab-0a02-454c-8d44-ced5667276ab	15
308657	benzocaine 20 % Mucous Membrane Topical Solution	SY	340ccdab-0a02-454c-8d44-ced5667276ab	15

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11822-0345-1	11822034501	14.7 g in 1 BOTTLE	14.7 g					Historical
11822-0345-7	11822034507	1 BOTTLE in 1 CARTON (11822-0345-7) / 14.7 g in 1 BOTTLE (11822-0345-1)	1 bottle	2015-01-01	2027-01-01	No	No	Historical
11822-0345-9	11822034509	1 BOTTLE in 1 CARTON (11822-0345-9) > 14.7 g in 1 BOTTLE (11822-0345-1)	1 bottle	2015-01-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
5820345 Rite Aid Max Str Oral Pain Relief	Rite Aid \| Lornamead Products \| HK KOLMAR CANADA, INC	2025-11-13	HUMAN OTC DRUG LABEL	15