FDA.reportPublic FDA data

85398-035-01 - Initial

Manufacturer
Beautivity LLC
Effective date
2026-09-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-19 01:00:37

Label at a glance#

ProductHermon Genital Herpes Symptoms Relief Cream
Active ingredientLEMONGRASS OIL, OLIVE OIL, WILLOW BARK
Label structure9 sections

Indications and uses

Temporarily relieves discomfort associated with genital herpes symptoms, including itching, tingling, burning, and skin irritation.

Dosage and administration

Adults and children 12 years and over: Clean and dry affected area before use. Apply a thin layer to affected area. Reapply as needed throughout the day. For best results, use at the earliest sign of symptoms. Children under 12 years: ask a doctor before use.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lemongrass 2X HPUS; Olive oil 3X HPUS; Willow bark 3X HPUS

Purpose

OTC - PURPOSE SECTION

Temporarily relieves discomfort associated with genital herpes symptoms.

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves discomfort associated with genital herpes symptoms, including itching, tingling, burning, and skin irritation.

Warnings

WARNINGS SECTION

For external use only. This product provides symptom relief only and is not intended to cure herpes. Use of this product will not prevent future outbreaks. This product is not intended to reduce transmission of herpes to others. This product does not protect against sexually transmitted infections (STIs).

Do not use

OTC - DO NOT USE SECTION

If you are allergic to any ingredient in this product.

When using this product

OTC - WHEN USING SECTION

Consult a healthcare professional before using this product. Apply only to the affected areas. Do not use in or near the eyes. Do not share this product with anyone; this may spread the infection or virus. Do not apply to severely irritated skin.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Symptoms worsen or persist after several days of use; excessive skin irritation or redness develops; or signs of an allergic reaction occur.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a healthcare professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and over: Clean and dry affected area before use. Apply a thin layer to affected area. Reapply as needed throughout the day. For best results, use at the earliest sign of symptoms. Children under 12 years: ask a doctor before use.

Other information

OTHER SAFETY INFORMATION

Store at room temperature and out of direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Leaf Water, Glycerin, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Dimethicone, Glyceryl Stearate, Polysorbate 60, Sorbitan Stearate, Panthenol, PEG-100 Stearate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, 1,2-Hexanediol, Hydroxyacetophenone, Beeswax, Butylene Glycol, Allantoin, Squalane, Salix Alba Bark Extract, Sorbitan Isostearate, Olea Europaea Leaf Extract, Cymbopogon Citratus Extract, Propanediol, Pentylene Glycol, Avena Strigosa Seed Extract.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hermon Genital Herpes Symptoms Relief Cream package label.
package labelpackage label

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85398-03585398-035-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
LEMONGRASS OIL5BIA40E9EDACTIB
OLIVE OIL6UYK2W1W1EACTIB
WILLOW BARKS883J9JDYXACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAF JUICERUE8E6T4NBIACT
GLYCERINPDC6A3C0OXIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
CETEARYL ALCOHOL2DMT128M1SIACT
DIMETHICONE92RU3N3Y1OIACT
GLYCERYL STEARATE230OU9XXE4IACT
POLYSORBATE 60CAL22UVI4MIACT
SORBITAN STEARATENVZ4I0H58XIACT
PANTHENOLWV9CM0O67ZIACT
PEG-100 STEARATEYD01N1999RIACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
BEESWAX2ZA36H0S2VIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ALLANTOIN344S277G0ZIACT
SQUALANEGW89575KF9IACT
SALIX ALBA BARK205MXS71H7IACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
OLEA EUROPAEA (OLIVE) LEAF POWDERMJ95C3OH47IACT
CYMBOPOGON CITRATUS WHOLE6AE8LT94NGIACT
PROPANEDIOL5965N8W85TIACT
PENTYLENE GLYCOL50C1307PZGIACT
AVENA STRIGOSA SEED4B6F760B0OIACT

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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