FDA.reportPublic FDA data

FEVANZON Cold Compress Medical Mask

Manufacturer
HBB INTERNATIONAL INC
Effective date
2020-10-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:11:58

Label at a glance#

ProductFEVANZON Cold Compress Medical Mask
Active ingredientSALICYLIC ACID
Label structure8 sections

Indications and uses

Anti-acne·Skin firming· Hydrating moisturizing.

Dosage and administration

Tear open the package and take out the mask, then apply onto the skin, press the non-woven mask lightly, each application time is 15-20 minutes

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Warnings

WARNINGS SECTION

For external use only.

  • Do not use on damaged or broken skin.
  • When using this product keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions :

DOSAGE & ADMINISTRATION SECTION

Tear open the package and take out the mask, then apply onto the skin, press the non-woven mask lightly, each application time is 15-20 minutes

Uses

INDICATIONS & USAGE SECTION

Anti-acne·Skin firming· Hydrating moisturizing.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water, glycerin, dipropylene glycol, Methyl Gluceth-20, niacinamide, dextrin, Piper methysticum root extract, Lonicera japonica (honeysuckle) flower extract, Scutellaria baicalensis root extract, Salvia miltiorrhiza root extract, hydroxyacetophenone, 1,2-hexanediol, tetrapeptide-2, nonapeptide-1, nicotinamide adenine dinucleotide, xanthan gum, sodium hyaluronate, disodium EDTA.

Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80815-00280815-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
DIPROPYLENE GLYCOLE107L85C40IACT
METHYL GLUCETH-20J3QD0LD11PIACT
NIACINAMIDE25X51I8RD4IACT
ICODEXTRIN2NX48Z0A9GIACT
PIPER METHYSTICUM ROOTBOW48C81XPIACT
LONICERA JAPONICA FLOWER4465L2WS4YIACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
SALVIA MILTIORRHIZA ROOT1693AM5SBNIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
TETRAPEPTIDE-27BQ5P2574KIACT
NONAPEPTIDE-164W45420K5IACT
DISODIUM NICOTINAMIDE ADENINE DINUCLEOTIDE8295030YNCIACT
XANTHAN GUMTTV12P4NEEIACT
HYALURONATE SODIUMYSE9PPT4THIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT

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
d2809b4b-993a-3b8d-e053-2995a90ab332146046c7-996f-43cd-8b5a-8efdb08bb39f2021-12-06WarningsExact identifier
spl set id: 146046c7-996f-43cd-8b5a-8efdb08bb39f

Reported adverse events (FAERS/openFDA)#

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