FDA.reportPublic FDA data

Repairing and Soothing Treatment Essence

Manufacturer
VESEN, INC
Effective date
2019-08-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:15:24

Label at a glance#

ProductRepairing and Soothing Treatment Essence
Active ingredientALLANTOIN
Label structure8 sections

Indications and uses

Soothe irritated and compromised skin, Promote the renewal of skin

Dosage and administration

Shake gently before use. After cleaning, apply daily, morning and evening (or as needed) all over the face. Massage gently with fingertips until it is absorbed or saturate cotton pads in essence and apply to area of concern, leave on for 10-15 min.

Label contents#

Full prescribing information#

active ingredients

OTC - ACTIVE INGREDIENT SECTION

Allantoin

Purpose

OTC - PURPOSE SECTION

Skin Protectant

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 (1-800-222-1222) right away.

Uses

INDICATIONS & USAGE SECTION

Soothe irritated and compromised skin, Promote the renewal of skin

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Propandiol, Glycerin, Betaine, Centella Asiatica (Gotu Kola) Leaf Extract, Salix Nigra (Willow) Bark extract, 1,2 hexandiol and Caprylyl glycol, Sodium Phytate, Citric acid.

Warnings

WARNINGS SECTION

For external use only

Do not use when skin is red, inflamed, irritated, or painful

When using this product

Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

Rash or irritation on skin develops and lasts

Directions

DOSAGE & ADMINISTRATION SECTION

Shake gently before use. After cleaning, apply daily, morning and evening (or as needed) all over the face. Massage gently with fingertips until it is absorbed or saturate cotton pads in essence and apply to area of concern, leave on for 10-15 min.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72575-10272575-102-01, 72575-102-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZACTIB
WATER059QF0KO0RIACT
CENTELLA ASIATICA7M867G6T1UIACT
GLYCERINPDC6A3C0OXIACT

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
cfe6a700-ae63-31bc-e053-2a95a90a101a9018371c-83c0-79f9-e053-2995a90a95682021-10-19WarningsExact identifier
spl set id: 9018371c-83c0-79f9-e053-2995a90a9568

Reported adverse events (FAERS/openFDA)#

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