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 36 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Acetaminophen	ACETAMINOPHEN	NuCare Pharmaceuticals,Inc.	872365ca-0c6b-550a-e053-2a91aa0ab25a	2024-06-14	Warnings	Exact identifier application number: M022
Amosan Oral Wound Cleanser Spearmint	SODIUM PERBORATE MONOHYDRATE	Vintage Brands Limited	7ac6c649-758f-4128-9920-466c0967b86a	2024-05-21	Warnings	Exact identifier application number: M022
Sensodyne	POTASSIUM NITRATE AND SODIUM FLUORIDE	Haleon US Holdings LLC	9e8e7b9f-3ccd-4935-b886-93f3a5045b67	2024-05-15	Warnings	Exact identifier application number: M022
Sensodyne Extra Whitening	POTASSIUM NITRATE AND SODIUM FLUORIDE	Haleon US Holdings LLC	1ed4a62b-f1d3-4740-8150-b94e02398740	2024-05-15	Warnings	Exact identifier application number: M022
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

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