Herpecin Pain Relief

Product NDC: 71687-4000
11-digit product format: 716874000
Labeler code: 71687
Product ID: 71687-4000_50b1a42a-3097-841b-e063-6294a90a0866
Type: HUMAN OTC DRUG
Nonproprietary name: Allantoin, Benzethonium Chloride, Lidocaine HCl
Dosage form: GEL
Route: TOPICAL
Labeler: Focus Consumer Healthcare, LLC
Application: M016
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-06-11
Substance: LIDOCAINE HYDROCHLORIDE ANHYDROUS; ALLANTOIN; BENZETHONIUM CHLORIDE
Active strength: 4; 2; .2 g/100g; g/100g; g/100g
Pharmacologic classes: Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
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 · 14 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
2025-04-01 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	71687-4000-1	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	71687-4000-1	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	71687-4000-1	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	71687-4000-1	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	71687-4000-1	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	71687-4000-1	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	71687-4000-1	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: Herpecin Pain Relief
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
LIDOCAINE HYDROCHLORIDE ANHYDROUS	4 g/100g
ALLANTOIN	2 g/100g
BENZETHONIUM CHLORIDE	.2 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
EC2CNF7XFP	Internal UNII lookup
344S277G0Z	Internal UNII lookup
PH41D05744	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2566834	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
beeb6043-6547-4fe9-e053-2995a90a5d74	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
860a93dc-4863-49cc-b284-6bbe8191bc48	Product name	4	20250214
eaba870a-6a9d-442e-8643-87b3f558a451	Product name	1	20250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86	Product name	1	20230117
fa8b5901-e681-426f-82fe-54f6d81ec698	Product name	4	20180619
332d03e4-aa24-4b11-841a-02bf41081920	Product name	1	20171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070	Product name	1	20171221
68ed98f8-24c2-44a0-944a-6d36e82ce25a	Product name	1	20141222
1cd42bc2-a430-c72b-636d-991b235fbf80	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71687-4000-1	2025-04-14	C162847	48780-1	2cef2736-9e59-d83d-e063-dadaa90ab31f	Herpecin Pain Relief
71687-4000-1	2025-01-30	C162847	48780-1	2cef2736-9e59-d83d-e063-dadaa90ab31f	Herpecin Pain Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71687-4000-1	Herpecin Pain Relief	1 in 1 CARTON	GEL	1		3
71687-4000-1	Herpecin Pain Relief	4 g in 1 TUBE	GEL	4		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71687-4000	HERPECIN PAIN RELIEF (ALLANTOIN, BENZETHONIUM CHLORIDE, LIDOCAINE HCL) GEL [FOCUS CONSUMER HEALTHCARE, LLC]	2	Current NDC, Legacy NDC, 2 package rows	20250416_beeb6043-6547-4fe9-e053-2995a90a5d74.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 2 of 68 · 1,357 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Petroleum Skin Protectant	WHITE PETROLATUM	Your Military Exchanges	1a0aed14-8606-4676-b4b5-23dd415d43ac	2026-09-02	Warnings, Adverse reactions	Exact identifier application number: M016
Aloetouch Protect Fragrance Free	DIMETHICONE	Medline Industries, LP	81f0071b-2bf3-455b-9e5d-8f3ca20adcdf	2026-09-01	Warnings	Exact identifier application number: M016
PURE PETROLATUM	PETROLATUM	VASA COSMETICS PRIVATE LIMITED	5a57b197-3e18-b3ab-e063-6394a90aed82	2026-08-31	Warnings	Exact identifier application number: M016
HYDROPHOR	HYDROPHOR	Akron Pharma Inc.	e6099df7-d418-479a-9d2e-ced523585aed	2026-08-28	Warnings	Exact identifier application number: M016
Witch Hazel	WITCH HAZEL	United Natural Foods, Inc. dba UNFI	d2d1bd9e-7025-4151-95f2-a2f521dc2be8	2026-08-28	Warnings, Adverse reactions	Exact identifier application number: M016
Daily Moisturizing	DIMETHICONE	Your Military Exchanges	e7af5488-1c49-41e9-9d8b-d519c6107699	2026-08-28	Warnings, Adverse reactions	Exact identifier application number: M016
Calamine	FERRIC OXIDE RED	Your Military Exchanges	af95a66c-f063-4019-80c6-6f7dc4fee4d8	2026-08-28	Warnings, Adverse reactions	Exact identifier application number: M016
Estriol Cream	ESTRIOL	Guangxi Keyun E-commerce Co., Ltd.	4deadcb6-0d46-bdd7-e063-6294a90a26d7	2026-08-27	Warnings	Exact identifier application number: M016
Medline	DIMETHICONE	Medline Industries, LP	0d964138-f68d-dbf5-e063-6294a90a8320	2026-08-27	Warnings	Exact identifier application number: M016
Gembooxt ECZEMA RELIEF Cream	HYDROCORTISONE	Guangdong Quadrant Ecological Technology Co., Ltd.	46490d65-f789-eaa2-e063-6294a90a623b	2026-08-27	Warnings	Exact identifier application number: M016
Serawise Eczema Relief	OATMEAL	DrAnaMaria. Com LLC	f0681436-d140-4e02-afe4-5b16de07afcd	2026-08-26	Warnings	Exact identifier application number: M016
Hair Regrowth Foam	GLYCERIN	Shantou Ouhoe Technology Co., Ltd.	59ef5953-e96f-5707-e063-6294a90a3094	2026-08-26	Warnings	Exact identifier application number: M016
Growth Treatment	GLYCERIN	Shantou Ouhoe Technology Co., Ltd.	59fe12eb-574f-a199-e063-6394a90abd06	2026-08-26	Warnings	Exact identifier application number: M016
Acne Relief	SALICYLIC ACID,NIACINAMIDE,PANTHENOL.	Guangzhou Senmai Biotechnology Co.,Ltd.	59db0143-de57-59d2-e063-6294a90a32a8	2026-08-25	Warnings	Exact identifier application number: M016
Witch Hazel	WITCH HAZEL	Your Military Exchanges	4079fd56-55f3-4e69-93e0-7590c07fb794	2026-08-25	Warnings, Adverse reactions	Exact identifier application number: M016
Salicylic Acid Acne Gel Cleanser	SALICYLIC ACID,PANTHENOL	Guangzhou Senmai Biotechnology Co.,Ltd.	59eb395b-493b-efc9-e063-6294a90aa891	2026-08-25	Warnings	Exact identifier application number: M016
Claravie	DIMETHICONE	Gentell LLC	59c6da39-b5f1-8253-e063-6394a90a0e8f	2026-08-24	Warnings	Exact identifier application number: M016
Medline	DIMETHICONE	Medline Industries, LP	0d94fd18-a120-e171-e063-6394a90ae9c0	2026-08-24	Warnings	Exact identifier application number: M016
MUSTELA Diaper Rash 1 2 3	ZINC OXIDE	Expanscience Laboratories d/b/a Mustela	59cf1d1e-e951-9d58-e063-6394a90af0f3	2026-08-24	Warnings	Exact identifier application number: M016
Claravie	ZINC OXIDE, DIMETHICONE	Gentell LLC	598a5c0b-1e2f-1335-e063-6394a90ac4f4	2026-08-21	Warnings	Exact identifier application number: M016

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
EC2CNF7XFP	LIDOCAINE HYDROCHLORIDE ANHYDROUS	73-78-9	LIDOCAINE HYDROCHLORIDE ANHYDROUS
344S277G0Z	ALLANTOIN	97-59-6	ALLANTOIN
PH41D05744	BENZETHONIUM CHLORIDE	121-54-0	BENZETHONIUM CHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2566834	allantoin 2 % / benzethonium chloride 0.2 % / lidocaine hydrochloride 4 % Oral Gel	PSN	beeb6043-6547-4fe9-e053-2995a90a5d74	3
2566834	allantoin 0.02 MG/MG / benzethonium chloride 0.002 MG/MG / lidocaine hydrochloride 0.04 MG/MG Oral Gel	SCD	beeb6043-6547-4fe9-e053-2995a90a5d74	3
2566834	allantoin 2 % / benzethonium chloride 0.2 % / lidocaine hydrochloride 4 % Oral Gel	SY	beeb6043-6547-4fe9-e053-2995a90a5d74	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
71687-4000-1	71687400001	1 TUBE in 1 CARTON (71687-4000-1) / 4 g in 1 TUBE	1 tube	2021-06-11	0000-00-00	No	No	Current