FDA.reportPublic FDA data

Herpetino Cold Sore Relief Terry Naturally Brand

Manufacturer
Gehrlicher Pharmazeutische Extrakte GmbH
Effective date
2019-07-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:17:46

Label at a glance#

ProductHerpetino Cold Sore Relief Terry Naturally Brand
Active ingredientALLANTOIN
Label structure6 sections

Indications and uses

• Relieves dryness and softens cold sores and fever blisters. • Softens scabs associated with cold sores and fever blisters. • Helps prevent, protect, and soothe chapped, cracked skin and lips.

Dosage and administration

Apply at first sign of cold sore or fever blister, several times daily.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Allantoin 1%

Purpose

OTC - PURPOSE SECTION

Cold sore/fever blister treatment and skin protectant

Uses

INDICATIONS & USAGE SECTION

• Relieves dryness and softens cold sores and fever blisters.
• Softens scabs associated with cold sores and fever blisters.
• Helps prevent, protect, and soothe chapped, cracked skin and lips.

Warnings

WARNINGS SECTION

For external use only.

When using this product 

OTC - WHEN USING SECTION

• Avoid contact with eyes.

Do not use on: 

OTC - DO NOT USE SECTION

• deep or puncture wounds • animal bites • serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

• Condition worsens • Symptoms last more than 7 days or clear up and occur again within a few days.

Keep out of the reach of children. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions:

DOSAGE & ADMINISTRATION SECTION

Apply at first sign of cold sore or fever blister, several times daily.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Bisabolol (Chamomile), Dimethicone, Hexyl Laurate, Jojoba (Simmondsia Chinensis) Seed Oil, Panthenol, Polyglyceryl-4 Isostearate, Polyisobutane, Propolis Extract, Shea (Butyrospermum Parkii) Butter, Sodium Chloride, Sweet Almond (Amygdalus Dulcis) Oil, Tocopheryl Acetate, Water, Xylitol.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelTubeTube

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72106-00072106-000-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHAMOMILEFGL3685T2XIACT
DIMETHICONE92RU3N3Y1OIACT
HEXYL LAURATE4CG9F9W01QIACT
JOJOBA OIL724GKU717MIACT
PANTHENOLWV9CM0O67ZIACT
POLYGLYCERYL-4 ISOSTEARATE820DPX33S7IACT
PROPOLIS WAX6Y8XYV2NOFIACT
SHEA BUTTERK49155WL9YIACT
SODIUM CHLORIDE451W47IQ8XIACT
ALMOND OIL66YXD4DKO9IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
XYLITOLVCQ006KQ1EIACT
ALLANTOIN344S277G0ZACTIB

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
8eea5a2c-f305-d1a3-e053-2995a90aab2798e2919e-5780-4f30-b40e-c5cb32e99f6d2019-07-30WarningsExact identifier
spl id: 8eea5a2c-f305-d1a3-e053-2995a90aab27
spl set id: 98e2919e-5780-4f30-b40e-c5cb32e99f6d

Reported adverse events (FAERS/openFDA)#

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