FEVANZON Revitalizing Lady Cream

Manufacturer
HBB INTERNATIONAL INC
Effective date
2020-10-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:11:48

Label at a glance#

ProductFEVANZON Revitalizing Lady Cream
Active ingredientOCTISALATE, OCTOCRYLENE
Label structure8 sections

Indications and uses

Brightening, firming, moisturizing, Anti-wrinkle

Dosage and administration

After cleansing the face, take proper amount of the product and spread evenly on the face, massage it lightly until it's absorbed into the skin.  It's suggested to be used before sunscreen lotion during the day.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octisalate ,Octocrylene.

Purposes

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Brightening, firming, moisturizing, Anti-wrinkle

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.
  • Due to the difference of our skin, this may not be for everyone, try it first on your sensitive part of skin, if any discomfort occurs, stop use right away.
  • Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Directions 

DOSAGE & ADMINISTRATION SECTION

  • After cleansing the face, take proper amount of the product and spread evenly on the face, massage it lightly until it's absorbed into the skin. 
  • It's suggested to be used before sunscreen lotion during the day.

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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, titanium dioxide, butylene glycol, Ethylhexyl methoxycinnamate, beeswax, glycerin, ethylhexyl palmitate, cetyl ethylhexanoate, mineral oil, C12-15 alkyl benzoate, caprylic/capric triglyceride, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, propylene glycol dicaprylate/dicaprate, hydroxystearic acid, sorbitan sesquioleate, sodium chloride, tetrapeptide-2, nonapeptide-1,palmitoyl oligopeptide, polyvinyl alcohol, xanthan gum,glyceryl caprylate, niacinamide, stearalkonium hectorite, propylene carbonate, triethoxycaprylylsilane, silica, methicone, nicotinamide adenine dinucleotide, 1,2-hexanediol, hydroxyacetophenone, PEG / PPG -17/6 copolymer, disodium EDTA, fragrance, iron oxides.

Product Image

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80815-00780815-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 41 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
d280aeed-dec5-03ba-e053-2a95a90a6b1c3883b4fb-4df7-4855-b2af-5ceb3e78aaae2021-12-06WarningsExact identifier
spl set id: 3883b4fb-4df7-4855-b2af-5ceb3e78aaae

Reported adverse events (FAERS/openFDA)#

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