Herpecin Pain Relief

Manufacturer
Focus Consumer Healthcare, LLC
Effective date
2026-04-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:55:47

Label at a glance#

ProductHerpecin Pain Relief
Active ingredientLIDOCAINE HYDROCHLORIDE ANHYDROUS, ALLANTOIN, BENZETHONIUM CHLORIDE
Label structure8 sections

Indications and uses

■ temporarily relieves pain and itching due to cold sores or fever blisters ■ temporarily relieves dryness; softens crusts (scabs) due to cold sores or fever blisters ■ first aid to help prevent infection

Dosage and administration

adults and children 12 years of age or older: ■ clean the affected area ■ apply a small amount of this product to the cold sore or fever blister 1 to 3 times daily children under 12 years of age: Ask a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Allantoin 2%
Benzethonium chloride 0.2%
Lidocaine HCl 4%

Purposes

OTC - PURPOSE SECTION

Skin Protectant

Antiseptic

Topical Anesthetic

Uses

INDICATIONS & USAGE SECTION

■ temporarily relieves pain and itching due to cold sores or fever blisters

■ temporarily relieves dryness; softens crusts (scabs) due to cold sores or fever blisters

■ first aid to help prevent infection

Warnings

WARNINGS SECTION

For external use only

For external use only

SPL UNCLASSIFIED SECTION

For external use only

DO NOT USE

OTC - DO NOT USE SECTION

Do not useover large areas of the body or on deep or puncture wounds, animal bites or serious burns

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

■ keep out of eyes. Rinse with water to remove.

■ apply only to the affected area. Avoid applying directly inside the mouth.

OTC - STOP USE SECTION

Stop use and ask a doctor ifrash occurs, or if condition worsens or symptoms persist more than 7 days or clear up and occur again in a few days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 12 years of age or older:

■ clean the affected area

■ apply a small amount of this product to the cold sore or fever blister 1 to 3 times daily

children under 12 years of age:Ask a doctor

Other information

SPL UNCLASSIFIED SECTION

■ protect this product from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice, bisabolol, disodium EDTA, ethylhexylglycerin, glycerin, hydrolyzed jojoba esters, hydroxyethylcellulose, lysine HCl, melissa officinalis extract, mentha piperita (peppermint) oil, mentha viridis (spearmint) leaf oil, potassium hydroxide, sclerotium gum, water, zingiber officinale (ginger) root extract

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Maximum Strength - NEW

Herpecin L

Pain Relief

Triple Action with Lidocain

Tageted Spot Treatment

for Cold Sores & Fever Blisters

Protects Against Infection

Numbs Cold Sore Pain & Itch at the Source

Helps Preven Cracking

Cold Sore Pain Reliever/Antiseptic/Lop Protectant Gel NET WT 0.15oz (4g)

Herpecin PainHerpecin Pain

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2566834allantoin 2 % / benzethonium chloride 0.2 % / lidocaine hydrochloride 4 % Oral GelPSN3
2566834allantoin 0.02 MG/MG / benzethonium chloride 0.002 MG/MG / lidocaine hydrochloride 0.04 MG/MG Oral GelSCD3
2566834allantoin 2 % / benzethonium chloride 0.2 % / lidocaine hydrochloride 4 % Oral GelSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130371687777333GTIN-13: 0371687777333
EAN-13: 0371687777333
GTIN-12: 371687777333
UPC-A: 371687777333
GTIN storage (14 digits): 00371687777333
Herpecin Pain.jpg
Data codeCode 1280412Herpecin Pain.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71687-4000-12025-04-14C16284748780-12cef2736-9e59-d83d-e063-dadaa90ab31fHerpecin Pain Relief
71687-4000-12025-01-30C16284748780-12cef2736-9e59-d83d-e063-dadaa90ab31fHerpecin Pain Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71687-4000-1Herpecin Pain Relief1 in 1 CARTONGEL13
71687-4000-1Herpecin Pain Relief4 g in 1 TUBEGEL43

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71687-400071687-4000-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Herpecin Pain ReliefALLANTOIN, BENZETHONIUM CHLORIDE, LIDOCAINE HCLFocus Consumer Healthcare, LLCbeeb6043-6547-4fe9-e053-2995a90a5d742026-04-30WarningsExact identifier
ndc (package): 71687-4000-1
ndc (product): 71687-4000
ndc11 (package): 71687400001
spl id: 50b1a42a-3097-841b-e063-6294a90a0866
spl set id: beeb6043-6547-4fe9-e053-2995a90a5d74

Reported adverse events (FAERS/openFDA)#

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