NDC 55346-2902-01 - Alpha-Caine Topical Anesthetic

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: 55346-2902
Requested NDC: 55346-2902-01
Package NDCs from labels: 55346-2902-1, 55346-2902-01
Manufacturer: Dental Technologies, Inc.
Effective date: 2025-11-04
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Alpha-Caine Drug Facts, Mint	Dental Technologies, Inc.	2025-11-04	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55346-2902-1	Alpha-CaineTopical Anesthetic	30 g in 1 BOTTLE, PLASTIC	GEL	30		9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55346-2902	ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.]	8	Current NDC, Legacy NDC, 1 package rows	20231216_ae628766-25b7-4b4f-abb8-a43faf2f44b9.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Benzocaine	ACTIVE INGREDIENT	U3RSY48JW5	ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.]	5
Benzocaine	ACTIVE MOIETY	U3RSY48JW5	ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.]	5
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.]	5
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.]	5
Polyethylene Glycol 3350	INACTIVE INGREDIENT	G2M7P15E5P	ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.]	5
Polyethylene Glycol 400	INACTIVE INGREDIENT	B697894SGQ	ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.]	5
SACCHARIN SODIUM	INACTIVE INGREDIENT	SB8ZUX40TY	ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.]	5

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 45 of 62 · 1,227 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Prevention Mouth Sore Rinse	HYDROGEN PEROXIDE	Prevention Health Sciences, Inc.	2eae61e4-1800-5fa6-e063-6394a90a9583	2025-01-01	Warnings	Exact identifier application number: M022
Antiseptic Lil Drug Store Products	EUCALYPTOL, MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, AND THYMOL	Lil' Drug Store Products, Inc	dca36a30-2c9f-4d0b-be88-b45c7046f509	2024-12-31	Warnings	Exact identifier application number: M022
Rite Aid Hydration Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Rite Aid Corporation	ecac1351-e944-21da-e053-2995a90a6d34	2024-12-31	Warnings	Exact identifier unii: B697894SGQ
Sensodyne Clinical White Intensive Clean	POTASSIUM NITRATE, SODIUM FLUORIDE	Haleon US Holdings LLC	f193ec40-032f-42c7-81f1-029ec8989374	2024-12-31	Warnings	Exact identifier application number: M022
BiteMD External Analgesic First Aid Antiseptic	BENZOCAINE, CAMPHOR (SYNTHETIC), AND PHENOL	United Industries Corporation	4c60db03-6d2b-4ae0-a200-718b3a50eb0f	2024-12-23	Warnings	Exact identifier unii: U3RSY48JW5
Glitch Advanced Relief Eye Drops	POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL	Misemer Pharmaceutical, Inc	03778509-3374-2168-e063-6294a90a9505	2024-12-23	Warnings	Exact identifier unii: B697894SGQ
TeethWhitening Kit	TEETHWHITENING KIT	Jiangxi Dentalbright Technology Co., Ltd.	29393313-217a-dc3a-e063-6294a90addb1	2024-12-20	Warnings	Exact identifier application number: M022
Breezers Cool Berry	PECTIN	Mondelez Global LLC	b31d0078-21d7-4d18-a8d3-7c8d48d6d004	2024-12-20	Warnings	Exact identifier application number: M022
Breezers Creamy Strawberry	PECTIN	Mondelez Global LLC	777fd6db-f129-4489-8312-4b1aca94878e	2024-12-20	Warnings	Exact identifier application number: M022
Halls Breezers Sugar Free Cool Berry	PECTIN	Mondelez Global LLC	dd1b4b17-4f73-4052-9589-d5fd6bb059bb	2024-12-20	Warnings	Exact identifier application number: M022
Mirakel Pain and Itch Relief	BENZOCAINE 20%, RESORCINOL 3%	Sanvio, Inc.	ed34d728-0275-e209-e053-2995a90a93ff	2024-12-20	Warnings	Exact identifier unii: U3RSY48JW5
Oral Gel Oral Pain Relief	BENZOCAINE BENZALKONIUM CHLORIDE	Savvy Care and Cosmetics	05ede7e4-5a0a-c942-e063-6294a90a8a24	2024-12-19	Warnings	Exact identifier application number: M022 unii: U3RSY48JW5
Pain, Burn, and Itch Relief	BENZOCAINE 20%, MENTHOL 0.5%	Derma Care Research Labs, LLC	fd9fe09f-3ae9-c5f5-e053-6394a90ad691	2024-12-19	Warnings	Exact identifier unii: U3RSY48JW5
EcoDent Ultimate Essential Mouthcare Sparkling Clean Mint	SODIUM BICARBONATE	Lotus Brands, Inc.	4a95c8c1-db7c-4791-ac58-3eac216a0126	2024-12-18	Warnings	Exact identifier application number: M022
EcoDent Ultimate Essential Mouthcare Spicy-Cool Cinnamon	SODIUM BICARBONATE	Lotus Brands, Inc.	6703b29d-cdc9-4c74-91c0-fb0c98dd043e	2024-12-18	Warnings	Exact identifier application number: M022
Red Cross Oral Pain Relief	BENZOCAINE	The Mentholatum Company	cbd41429-f730-4577-9f06-ef1831cf62e1	2024-12-17	Warnings	Exact identifier application number: M022 unii: U3RSY48JW5
Red Cross Canker Sore	BENZOCAINE	The Mentholatum Company	54cfff96-6665-4b36-a15d-10bf6cf3a1f9	2024-12-17	Warnings	Exact identifier application number: M022 unii: U3RSY48JW5
Chiggerex	BENZOCAINE	RANDOB LABS, LTD. DBA CROSSINGWELL CONSUMER HEALTH	5e5d84ab-f57f-448d-a4c1-ced38890eec2	2024-12-17	Warnings	Exact identifier unii: U3RSY48JW5
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 unii: U3RSY48JW5

Reported adverse events (FAERS/openFDA)#

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