FEVANZON Polypeptide Revitalizing Essence Emulsion

FEVANZON Polypeptide Revitalizing Essence Emulsion by

Drug Labeling and Warnings

FEVANZON Polypeptide Revitalizing Essence Emulsion by is a Otc medication manufactured, distributed, or labeled by HBB INTERNATIONAL INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

FEVANZON POLYPEPTIDE REVITALIZING ESSENCE EMULSION- avobenzone,octisalate,octocrylene emulsion 
HBB INTERNATIONAL INC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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FEVANZON Polypeptide Revitalizing Essence Emulsion

Active Ingredients

Avobenzone,Octisalate,Octocrylene

Purpose

sunscreen

Warnings

• 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 skin, this product 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.

Keep out of reach of children.

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

Directions :

• After cleansing the face, take proper amount of the product and spread evenly on the face, massage it lightly until it's absorbed.

Uses

Brightening·Anti-wrinkle Essence·Hydrate Nutrition.

Other Infomation

Store at room temperature without direct sunshine.

Inactive Ingredient

Water, glycerin, cyclopentasiloxane, butylene glycol, dimethicone, hydroxyethyl urea, Helianthus annuus (sunflower) seed oil, arachidyl alcohol, behenyl alcohol, arachidyl glucoside, acetyl hexapeptide-8, palmitoyl oligopeptide, pentylene glycol, hydroxyphenyl propamidobenzoic acid, ascorbyl palmitate, dimethyl isosorbide, hydroxypinacolone retinoate, tetrapeptide-2, nonapeptide-1, palmitoyl oligopeptide, polyvinyl alcohol, glyceryl caprylate, nicotinamide adenine dinucleotide, 1,2-hexanediol, hydroxyacetophenone, silica, methicone, sodium acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, Polysorbate 80, arginine, acrylates/C10-30 alkyl acrylate crosspolymer, allantoin, xanthan gum, sodium hyaluronate, polyvinyl alcohol, glyceryl caprylate, chlorphenesin, fragrance

Product Label

FEVANZON POLYPEPTIDE REVITALIZING ESSENCE EMULSION 
avobenzone,octisalate,octocrylene emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80815-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
DIMETHICONE (UNII: 92RU3N3Y1O)
HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)
SUNFLOWER OIL (UNII: 3W1JG795YI)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
DOCOSANOL (UNII: 9G1OE216XY)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)
TETRAPEPTIDE-2 (UNII: 7BQ5P2574K)
NONAPEPTIDE-1 (UNII: 64W45420K5)
DISODIUM NICOTINAMIDE ADENINE DINUCLEOTIDE (UNII: 8295030YNC)
NADIDE (UNII: 0U46U6E8UK)
HYDROXYPINACOLONE RETINOATE (UNII: NJ3V2F02E1)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
METHICONE (20 CST) (UNII: 6777U11MKT)
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
ISOHEXADECANE (UNII: 918X1OUF1E)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
ARGININE (UNII: 94ZLA3W45F)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
.MU.-CONOTOXIN G IIIC (UNII: 3T2U70084B)
XANTHAN GUM (UNII: TTV12P4NEE)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
CHLORPHENESIN (UNII: I670DAL4SZ)
FRAGRANCE FLORAL ORC0902236 (UNII: R66Z4YW3X0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80815-006-01	50 in 1 CARTON	08/22/2020	08/22/2020
1		100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	08/22/2020	08/22/2020

Labeler - HBB INTERNATIONAL INC (117557618)

Revised: 12/2021

Document Id: d2809b4b-996b-3b8d-e053-2995a90ab332

34390-5

Set id: 6ad5fbe5-cb8c-4a14-92f4-7d2546abf230

Version: 3

Effective Time: 20211206