Gumsol

Product NDC: 52083-714
11-digit product format: 520830714
Labeler code: 52083
Product ID: 52083-714_df716e50-f0a6-4548-b354-29dd8c29924c
Type: HUMAN OTC DRUG
Nonproprietary name: Benzocaine, Zinc Chloride
Dosage form: SPRAY
Route: ORAL
Labeler: Kramer Novis
Application: M022
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2014-02-28
Substance: BENZOCAINE; ZINC CHLORIDE
Active strength: 1.5; .03 g/30mL; g/30mL
Pharmacologic classes: Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 · 16 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
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	52083-714-01	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	52083-714-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	52083-714-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	52083-714-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	52083-714-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	52083-714-01	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	52083-714-01	U	Excluded because listing certification expired	`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	52083-714-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: Gumsol
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZOCAINE	1.5 g/30mL
ZINC CHLORIDE	.03 g/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
U3RSY48JW5	Internal UNII lookup
86Q357L16B	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
485558	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
3bb651d9-d1c4-4c25-bcfc-cd13e2f0d3bf	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f47a510b-6679-4664-b2d6-47b5c4afe7cc	Product name	4	20260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61c	Product name	2	20250515
0306390c-dd77-4363-afe0-63c58088b2a1	Product name	1	20220120
503ea967-4b9c-48cf-9e87-c7975295849d	Product name	2	20220120
190f2a5b-bbc8-65c7-fcb0-97891307b917	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52083-714-01	2025-11-18	C162847	48780-1	2cef2736-9d02-d83d-e063-dadaa90ab31f	GUMSOL
52083-714-01	2025-01-30	C162847	48780-1	2cef2736-9d02-d83d-e063-dadaa90ab31f	GUMSOL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52083-714-01	Gumsol	30 mL in 1 BOTTLE	SPRAY	30		3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
52083-714-01	ML - Milliliter	52083-714	a3d40f00-3276-485a-b753-8b0f10a9ed8f	1	2014-04-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BENZOCAINE	ACTIVE INGREDIENT	U3RSY48JW5	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	1
ZINC CHLORIDE	ACTIVE INGREDIENT	86Q357L16B	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	1
BENZOCAINE	ACTIVE MOIETY	U3RSY48JW5	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	1
ZINC CATION	ACTIVE MOIETY	13S1S8SF37	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	1
ASPARTAME	INACTIVE INGREDIENT	Z0H242BBR1	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	1
CETYLPYRIDINIUM CHLORIDE	INACTIVE INGREDIENT	D9OM4SK49P	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	1
MENTHOL	INACTIVE INGREDIENT	L7T10EIP3A	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	1
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	1
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52083-714	GUMSOL (BENZOCAINE, ZINC CHLORIDE) SPRAY [KRAMER NOVIS]	2	Current NDC, Legacy NDC, 1 package rows	20181211_3bb651d9-d1c4-4c25-bcfc-cd13e2f0d3bf.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 18 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Listerine Essential Care	SODIUM MONOFLUOROPHOSPHATE	Kenvue Brands LLC	90b5c3d8-baa4-44ab-8f73-e177007f0219	2025-10-10	Warnings	Exact identifier application number: M022
DuoCare Clinical Oral Rinse	CETYLPYRIDINIUM CHLORIDE	Medline Industries, LP	98e61cd5-7e29-7066-e053-2a95a90afa21	2025-10-10	Warnings	Exact identifier application number: M022
4-in-1 Teeth Care Pens	4-IN-1 TEETH CARE PENS	Jiangxi Dentalbright Technology Co., Ltd	40b756b7-ce1b-6482-e063-6294a90a0425	2025-10-09	Warnings	Exact identifier application number: M022
Giltuss Bucalsep	BENZOCAINE, MENTHOL, ZINC CHLORIDE	Gil Pharmaceutical Corp	85053391-8d71-ab4f-e053-2991aa0a7e08	2025-10-09	Warnings	Exact identifier application number: M022
Listerine Gum Therapy Mouthwash Glacier Mint	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Kenvue Brands LLC	40a0bdf3-1698-1449-e063-6394a90ab13d	2025-10-08	Warnings	Exact identifier application number: M022
Kalaya Breath Refresh	MOUTHWASH	Avaria Health and Beauty Corp	750e99ff-72e4-3c2f-e053-2a91aa0ad5a0	2025-10-08	Warnings	Exact identifier application number: M022
Trader Joes	SODIUM FLUORIDE 0.24% AND POTASSIUM NITRATE 5%	TRADER JOE'S COMPANY	159abeba-6da2-2643-e063-6394a90a730d	2025-10-08	Warnings	Exact identifier application number: M022
Family Wellness Oral Pain Relief	BENZOCAINE 20%	FAMILY DOLLAR SERVICES INC	105d87d6-9147-43d4-e063-6394a90a57ee	2025-10-08	Warnings	Exact identifier application number: M022
Equate Glistening Mint	SODIUM FLUORIDE	Walmart Inc.	39ff21ee-a362-014e-e063-6294a90a0d91	2025-10-03	Warnings	Exact identifier application number: M022
Mouth Sore Relief Professional Strength	BENZOCAINE	CVS Pharmacy	1b7209f6-8368-47fa-8df2-b049613b8c1b	2025-09-30	Warnings	Exact identifier application number: M022
Hydrogen Peroxide	HYDROGEN PEROXIDE	Family Dollar (FAMILY WELLNESS)	9db73da2-5b70-41e6-bcf9-caa7f1142024	2025-09-29	Warnings	Exact identifier application number: M022
Esunix Oral Bacteriostatic Liquid	CETYLPYRIDINIUM CHLORIDE	Xiling (Zhenjiang) Medical Technology Co., Ltd.	3f47d7e1-b6ae-efd1-e063-6394a90a4602	2025-09-27	Warnings	Exact identifier application number: M022
Chloraseptic Sore Throat Cherry	PHENOL	Prestige Brands Holdings, Inc.	d5d62f7a-8f92-4d42-a2fb-691f896f72fc	2025-09-26	Warnings	Exact identifier application number: M022
Giltuss Bucalsep	BENZOCAINE, MENTHOL, ZINC CHLORIDE	Dextrum Laboratories Inc.	3fa233dc-156c-1e95-e063-6294a90a8bbd	2025-09-25	Warnings	Exact identifier application number: M022
Finafta MultiOral	BENZOCAINE	Dextrum Laboratories Inc.	cb027ab8-4175-4cc0-a73e-991dfb113df9	2025-09-23	Warnings	Exact identifier application number: M022
4-in-1 Teeth Care Pens	4-IN-1 TEETH CARE PENS	Jiangxi Dentalbright Technology Co., Ltd	3f872924-0c44-267b-e063-6394a90a1a67	2025-09-23	Warnings	Exact identifier application number: M022
Dental Relief	BENZOCAINE	Cintas Corporation	0f40f775-797e-43cf-88c9-00eea666494f	2025-09-23	Warnings	Exact identifier application number: M022
Seavue Anti-caries Gel	SODIUM FLUORIDE	Xiling (Zhenjiang) Medical Technology Co., Ltd.	3f4c6086-b96d-8fa4-e063-6294a90ad800	2025-09-21	Warnings	Exact identifier application number: M022
Seavue Dental Desensitizer	POTASSIUM NITRATE AND SODIUM FLUORIDE DENTIFRICE	Xiling (Zhenjiang) Medical Technology Co., Ltd.	3f47f399-1a14-5264-e063-6394a90aeb1c	2025-09-20	Warnings	Exact identifier application number: M022
Povi-One	POVIDONE-IODINE 10% TOPICAL	Elevate Oral Care	27c29a33-d1cc-d72f-e063-6394a90a4d45	2025-09-19	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
86Q357L16B	ZINC CHLORIDE	7646-85-7	ZINC CHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
485558	benzocaine 5 % / zinc chloride 0.1 % Mucosal Spray	PSN	3bb651d9-d1c4-4c25-bcfc-cd13e2f0d3bf	3
485558	benzocaine 50 MG/ML / zinc chloride 1 MG/ML Mucosal Spray	SCD	3bb651d9-d1c4-4c25-bcfc-cd13e2f0d3bf	3
485558	benzocaine 5 % / zinc chloride 0.1 % Mucosal Spray	SY	3bb651d9-d1c4-4c25-bcfc-cd13e2f0d3bf	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
52083-714-01	52083071401	30 mL in 1 BOTTLE (52083-714-01)	30 ml	2014-02-28	0000-00-00	No	No	Current