Benzocaine

Product NDC: 71888-101
11-digit product format: 718880101
Labeler code: 71888
Product ID: 71888-101_47fac2e8-50dd-cddf-e063-6394a90a9176
Type: HUMAN OTC DRUG
Nonproprietary name: Benzocaine
Dosage form: GEL
Route: TOPICAL
Labeler: Bellus Medical, LLC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2017-06-01
Substance: BENZOCAINE
Active strength: 200 mg/mL
Pharmacologic classes: Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag: No
Listing certified through: 2027-12-31
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 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	71888-101-02	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	71888-101-02	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	71888-101-02	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	71888-101-02	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	71888-101-02	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	71888-101-02	`9bebd1f3094a…`	`5416666fcb17…`

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: Benzocaine
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZOCAINE	200 mg/mL

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
452688	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
60cafbaf-8ec6-46a5-e053-2a91aa0af11f	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2023-10-27	20% Benzocaine Gel
2023-10-27	20% Benzocaine Gel
2020-01-31	20% Benzocaine Gel
2020-01-31	20% Benzocaine Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71888-101-01	Benzocaine	4 mL in 1 PACKET	GEL	4		4
71888-101-02	Benzocaine	12 in 1 BOX	GEL	12		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71888-101	BENZOCAINE GEL [BELLUS MEDICAL, LLC]	3	Current NDC, Legacy NDC, 2 package rows	20241120_60cafbaf-8ec6-46a5-e053-2a91aa0af11f.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 16 of 156 · 3,115 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Warm Patch Tong Gu Huo Luo Gao	PAIN PATCH	Sheng Chang Pharmaceutical Co, Ltd. Zhongli Factory	6906c4a0-1557-45e3-b915-80e4dd652ee7	2026-06-10	Warnings	Exact identifier application number: M017
LidoMedix	LIDOCAINE, MENTHOL, CAMPHOR	Absolute Therapeutics, LLC	53d504ef-eea3-6a47-e063-6394a90a1f65	2026-06-09	Warnings	Exact identifier application number: M017
good sense anti itch	HYDROCORTISONE	Preferred Pharmaceuticals Inc.	e51047da-8e17-4dd7-be3c-54820a7485f2	2026-06-09	Warnings	Exact identifier application number: M017
Terramed Just Think Comfort GynoCare BV Guard Intimate Wash	PRAMOXINE HYDROCHLORIDE	Rida LLC	09964550-049c-4c3b-817d-37e660c2e45c	2026-06-08	Warnings	Exact identifier application number: M017
Quality Choice Lidocaine Pain Relief Patch	LIDOCAINE	Quality Choice (CHAIN DRUG MARKETING ASSOCIATION)	526abe69-4bbc-6e73-e063-6394a90ad25d	2026-06-08	Warnings	Exact identifier application number: M017
Dcsily Numbing Cream	LIDOCAINE	Shenzhen Xinxin Yunhai Technology Co., Ltd.	53cab09c-6d5d-471e-e063-6294a90aa977	2026-06-08	Warnings	Exact identifier application number: M017
Easment 0.1% Capsaicin cream for sensitive skin	CAPSAICIN 0.1%	Easment LLC	537e0106-9e1c-66b8-e063-6294a90ac538	2026-06-05	Warnings	Exact identifier application number: M017
RAVYNDRA Magnesium Cream	MENTHOL, CAMPHOR	Guangzhou Xinhongda Trading Service Co., Ltd.	532e2f62-0fb1-05b1-e063-6394a90ae538	2026-06-04	Warnings	Exact identifier application number: M017
Maximum Strength Pain Relief	MENTHOL CREAM	OWELL NATURALS LLC	5388f2c5-8cfd-a601-e063-6294a90a2e5f	2026-06-04	Warnings	Exact identifier application number: M017
RAVYNDRA Lidocaine 5% Numbing Cream	LIDOCAINE, WITCH HAZEL	Guangzhou Xinhongda Trading Service Co., Ltd.	535450d9-9fa9-0568-e063-6294a90a1075	2026-06-03	Warnings	Exact identifier application number: M017
MG PLUS ROLL ON	MENTHOL ROLL ON	RENU LABORATORIES, LLC	535dc42f-38c7-2afc-e063-6294a90ae23d	2026-06-03	Warnings	Exact identifier application number: M017
OP First Aid Series Insect Sting Relief Pad	BENZOCAINE, ISOPROPYL ALCOHOL	Yiwu Ori-Power Medtech Co.,Ltd.	b43af183-834a-0f64-e053-2995a90a3218	2026-06-03	Warnings	Exact identifier application number: M017
PURE PRIMAL DELAY	LIDOCAINE HCL	Prodigy Media Inc	1ddab664-7c44-452f-854f-e386cd69505e	2026-06-03	Warnings	Exact identifier application number: M017
Mineral Ice Extreme Dry Stick	MENTHOL	Carlin Consumer Health LLC	4f81be91-92e5-1205-e063-6394a90a6e82	2026-06-02	Warnings	Exact identifier application number: M017
Kalaya Extra Strength Pain Relief Gel with Arnica	METHYL SALICYLATE, MENTHOL, CAMPHOR	Avaria Health & Beauty Corp	b6a6237d-b471-4102-b5df-fc389f5f9258	2026-06-02	Warnings	Exact identifier application number: M017
Biofreeze Ultraflex	LIDOCAINE	Reckitt Benckiser LLC	2655974b-a67d-9f07-e063-6294a90a54e8	2026-06-02	Warnings	Exact identifier application number: M017
Biofreeze Ultraflex Plus	LIDOCAINE, MENTHOL	Reckitt Benckiser LLC	401e1843-e9a6-fda9-e063-6294a90a3073	2026-06-02	Warnings	Exact identifier application number: M017
Pain Relief	MENTHOL SPRAY	Owell Naturals Brand, LLC	534c871c-da35-6135-e063-6294a90aa9f6	2026-06-02	Warnings	Exact identifier application number: M017
Charm Tex FLUORIDE Gel	SODIUM FLUORIDE	Jiangsu Gold Worldworks Household Chemicals Co., Ltd.	09d47bd7-1438-4ef2-85e0-9cd5eb2f763a	2026-05-31	Warnings	Exact identifier application number: M017
Charm Tex FLUORIDE	SODIUM MONOFLUOROPHOSPHATE	Jiangsu Gold Worldworks Household Chemicals Co., Ltd.	2bddc69a-0c0f-47fc-bc98-90c2ec70dd6f	2026-05-31	Warnings	Exact identifier application number: M017

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
452688	benzocaine 20 % Topical Gel	PSN	60cafbaf-8ec6-46a5-e053-2a91aa0af11f	4
452688	benzocaine 0.2 MG/MG Topical Gel	SCD	60cafbaf-8ec6-46a5-e053-2a91aa0af11f	4
452688	benzocaine 20 % Topical Gel	SY	60cafbaf-8ec6-46a5-e053-2a91aa0af11f	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
71888-101-01	71888010101	4 mL in 1 PACKET	4 ml				Historical
71888-101-02	71888010102	12 PACKET in 1 BOX (71888-101-02) / 4 mL in 1 PACKET (71888-101-01)	12 packet	2017-06-01	No	No	Current