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 31 of 40 · 782 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Red Cross Canker Sore	BENZOCAINE	The Mentholatum Company	54cfff96-6665-4b36-a15d-10bf6cf3a1f9	2024-12-17	Warnings	Exact identifier application number: M022
Benzoin Tincture	BENZOIN RESIN	116956644	2981217f-f250-c090-e063-6294a90a85b0	2024-12-17	Warnings	Exact identifier application number: M022
Kank-A Mouth Pain	BENZOCAINE	Blistex Inc.	eebc03ba-f849-4e70-a653-834f383b6aa4	2024-12-17	Warnings	Exact identifier application number: M022
Topicale	BENZOCAINE	Medical Products Laboratories, Inc.	8282a4a6-b77c-75fc-e053-2991aa0ad4ac	2024-12-16	Warnings	Exact identifier application number: M022
Topicale Xtra	BENZOCAINE	Medical Products Laboratories,Inc.	9452bff4-8c08-eff9-e053-2a95a90a67ed	2024-12-16	Warnings	Exact identifier application number: M022
PHENOL	PHENOL	CHAIN DRUG MARKETING ASSOCIATION INC.	2379e23a-72fe-4e94-9d7e-9b623c0db174	2024-12-13	Warnings	Exact identifier application number: M022
KANKA SoftBrush	BENZOCAINE AND ZINC CHLORIDE	Blistex Inc	093f3545-1d8e-48a3-a533-e9c3ae6d740b	2024-12-12	Warnings	Exact identifier application number: M022
Topicale	BENZOCAINE	Medical Products Laboratories, Inc.	826eaef8-4457-3dc2-e053-2991aa0a528b	2024-12-11	Warnings	Exact identifier application number: M022
Topicale	BENZOCAINE	Medical Products Laboratories, Inc.	8281700c-10f9-841c-e053-2991aa0a918f	2024-12-11	Warnings	Exact identifier application number: M022
Topicale	BENZOCAINE	Medical Products Laboratories, Inc.	82824416-80de-76bd-e053-2a91aa0ad8b5	2024-12-11	Warnings	Exact identifier application number: M022
Topicale Xtra	BENZOCAINE	Medical Products Laboratories,Inc.	e3da0e63-a891-72bd-e053-2a95a90a58bc	2024-12-11	Warnings	Exact identifier application number: M022
Topicale Xtra	BENZOCAINE	Medical Products Laboratories, Inc.	e3d924b5-0788-46d3-e053-2995a90a027b	2024-12-11	Warnings	Exact identifier application number: M022
Fluoride Bits	SODIUM MONOFLUOROPHOSPHATE 0.76%	The Kind Lab, Inc.	fa433031-7376-0e5b-e053-6394a90a5f75	2024-12-11	Warnings	Exact identifier application number: M022
Fluoride Bits	SODIUM MONOFLUOROPHOSPHATE 0.76%	The Kind Lab, Inc.	eedf13dc-a009-027a-e053-2995a90a8ec8	2024-12-11	Warnings	Exact identifier application number: M022
NATURAL LEMON MINT HERB THROAT DROPS	MENTHOL	Ricola USA Inc.	763e8234-60be-4b1f-9f78-01c574f35d0a	2024-12-10	Warnings	Exact identifier application number: M022
Natural Cherry Honey Herb Throat Drops	MENTHOL	Ricola USA Inc.	989f8509-cd28-48e7-9aa1-baddfbcac95a	2024-12-10	Warnings	Exact identifier application number: M022
ORGANIC PEPPERMINT HERB THROAT DROPS	MENTHOL	Ricola USA Inc.	f75c8967-40e6-473a-b403-941354cb0be1	2024-12-10	Warnings	Exact identifier application number: M022
Natural Cherry Honey Herb Throat Drops	MENTHOL	Ricola USA Inc.	c56be34d-1dd5-4200-9723-3a73180cb759	2024-12-10	Warnings	Exact identifier application number: M022
Cherry Throat Drops	MENTHOL	Ricola USA Inc.	89257ceb-af0f-4516-88f7-6dfdab9e14f4	2024-12-10	Warnings	Exact identifier application number: M022
BERRY MEDLEY THROAT DROPS	MENTHOL	Ricola USA Inc.	9bfd2ea7-745b-47f8-bd8a-9dbeeaad8b95	2024-12-10	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