FDA.reportPublic FDA data

Herpes Relief Cream

Manufacturer
Ehy Holdings LLC
Effective date
2023-01-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:53:12

Label at a glance#

ProductHerpes Relief Cream
Active ingredientGRAPHITE
Label structure14 sections

Dosage and administration

Adult and children over 12 vears or old. Wash handsbefore and after applying the cream. Apply to affected area at the firstsign of blisters, sores, or tingling sensation. Rub in gently andthoroughly. Do not use more than 3 times daily. Children under 12years: ask a docto

Storage and handling

Store at room temperature and out of directsunlight.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Graphites 1%

Purpose

OTC - PURPOSE SECTION

Relief for skin eruptions, itchingin genital area

Use

INDICATIONS & USAGE SECTION

for the treatment ofsymptoms of herpes

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

Do not use morethan 3 times daily. Children under12 years: ask a docto

OTC - WHEN USING SECTION

When using this productavoid contact with eyes.lf contact occurs, rinse the eyesthoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens or does not improve

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adult and children over 12 vears or old. Wash handsbefore and after applying the cream. Apply to affected area at the firstsign of blisters, sores, or tingling sensation. Rub in gently andthoroughly. Do not use more than 3 times daily. Children under 12years: ask a docto

Other information

STORAGE AND HANDLING SECTION

Store at room temperature and out of directsunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Artemisia extractsSophora Flavescens, Cnidium Monnieri (L.) Cuss., Kochiascoparia, Dictamni Cortex, Smilax Glabra Roxb, SolidagoDecurrens, Phellodendron amurense Ruprecht., GleditsiaSinensis.

OTC - ASK DOCTOR SECTION

When using this product avoid contact with eyeslf contact occurs, rinse the eves thoroughly with water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

81799-005-1

1

81799-005-1 181799-005-1 1

81799-005-1

2

81799-005-1 281799-005-1 2

81799-005-1

3

81799-005-1 381799-005-1 3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81799-005-012024-07-30C16284748780-11030e365-5493-111a-e063-dadaa90a10e281799-005 Herpes Relief Cream
81799-005-012024-01-30C16284748780-11030e365-5493-111a-e063-dadaa90a10e281799-005 Herpes Relief Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81799-005-01Herpes Relief Cream60 g in 1 BOTTLECREAM601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81799-005HERPES RELIEF CREAM (ROYCEDERM HERPES RELIEF CREAM) CREAM [EHY HOLDINGS LLC]1Legacy NDC, 1 package rows20230112_f209ee77-d290-1203-e053-2a95a90adb8c.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81799-00581799-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
DICTAMNUS DASYCARPUS ROOT6153LEN214IACT
WATER059QF0KO0RIACT
WORMWOODF84709P2XVIACT
SMILAX GLABRA WHOLEH51N91QNEBIACT
GRAPHITE4QQN74LH4OACTIB
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT
BASSIA SCOPARIA POLLEN07A108ZKW5IACT
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT

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
f209ee77-d28f-1203-e053-2a95a90adb8cf209ee77-d290-1203-e053-2a95a90adb8c2023-01-11WarningsExact identifier
spl id: f209ee77-d28f-1203-e053-2a95a90adb8c
spl set id: f209ee77-d290-1203-e053-2a95a90adb8c

Reported adverse events (FAERS/openFDA)#

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