RoyceDerm Herpes RELIEF CREAM-194

Manufacturer
RoyceDerm LLC
Effective date
2026-05-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-15 00:32:40

Label at a glance#

ProductRoyceDerm Herpes RELIEF .cream
Active ingredientWILLOW BARK, OLIVE OIL, LEMONGRASS OIL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lemon grass 2X HPUS

Olive Extract 3X HPUS

Willow Bark Extract 3X HPUS

OTC - PURPOSE SECTION

Antiviral agent

Healingagent

Pain relief

DOSAGE & ADMINISTRATION SECTION

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

WARNINGS SECTION

For external use only.

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

Do not use If youare allergic to any ingredient in this product.

When using this product

  • 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/virus.
  • do not apply to severely irritated skin.

Stop use and ask a doctor if

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical helpor contact the Poison Control Center right away.

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a healthcare professional before use.

INDICATIONS & USAGE SECTION

Adults and children12 years and older:

  • Clean and dry the affected area before use.
  • Apply a thin layer to the 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 SAFETY INFORMATION

store at room temperature and out of direct sunlight.

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Leaf Water,Glycerin, Caprylic/Capric Triglyceride,Cetearyl Alcohol, Dimethicone,Glyceryl Stearate, Polysorbate 60,Panthenol, Sorbitan Stearate,PEG-100 Stearate, 1,2-Hexanediol,Hydroxyacetophenone, Beeswax,Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Butylene Glycol,Squalane, Allantoin, Propanediol,1,2-Pentanediol, Avena Strigosa Seed Extract.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packagepackage

Products#

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DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85424-02585424-025-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 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
52dd572c-2826-8398-e063-6294a90a3f9152dd572c-2825-8398-e063-6294a90a3f912026-05-28WarningsExact identifier
spl id: 52dd572c-2826-8398-e063-6294a90a3f91
spl set id: 52dd572c-2825-8398-e063-6294a90a3f91

Reported adverse events (FAERS/openFDA)#

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