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Mzank Sunscreen Daily Ultimate Protection Spf50 drug information

SUNSCREEN SPF50
Guangzhou Meixi Biotechnology Co., Ltd. · EXTRACORPOREAL

Product NDC: 84167-828

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameSUNSCREEN SPF50
Labeler / manufacturerGuangzhou Meixi Biotechnology Co., Ltd.
RouteEXTRACORPOREAL
Drug classDrug class not supplied in source label
Product NDC84167-828
Label effective date2026-08-27

Official product label reference

Mzank Sunscreen Daily Ultimate Protection Spf50 — Guangzhou Meixi Biotechnology Co., Ltd.

This page contains 7 source sections for SUNSCREEN SPF50, extracorporeal route. Label set 5a0b4bd2-f6ad-35dc-e063-6294a90a8a66, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

UsesHelps prevent sunburn,If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Purpose

Effectively blocks ultraviolet raysHelps protect skin from UVA& UVB damageLeaves skin feeling fresh andhydrated.
Dosage and administration — label text
36 Sachets, Net Wt. 0.11 oz (3 g) each Total Net Wt. 3.81 oz.(108g)
Warnings
Keep out of reach of children.
Active ingredient
Bemotrizinol，Ensulizole，Homosalate，Octisalate，Octocrylene，Titanium dioxide
Inactive ingredient
WATER,DIBUTYL ADIPATE,CETYL ETHYLHEXANOATE,GLYCERIN,DIPROPYLENE GLYCOL,ETHYLHEXYL STEARATE,C14-22 ALCOHOLS,DIMETHICONE,GLYCERYL STEARATE,1,2-HEXANEDIOL,HYDROXYACETOPHENONE,POTASSIUM CETYL PHOSPHATE,HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER,C12-20 ALKYL GLUCOSIDE,PEG-100 STEARATE,SODIUM HYDROXIDE,ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER,TRIETHANOLAMINE,SILICA,XANTHAN GUM,ALLANTOIN,FRAGRANCE,BISABOLOL,TOCOPHERYL ACETATE,DISODIUM EDTA,POLYSORBATE 60,SORBITAN ISOSTEARATE,BUTYLENE GLYCOL,PROPANEDIOL,LEONTOPODIUM ALPINUM FLOWER/LEAF EXTRACT,BUDDLEJA OFFICINALIS EXTRACT,SCUTELLARIA ALPINA FLOWER/LEAF/STEM EXTRACT,THEOBROMA CACAO (COCOA) SEED EXTRACT,CITRIC ACID
Child safety
apply liberally and evenly 15 minutes before sun exposure.

Official sources and product identifiers

Substances listed: BEMOTRIZINOL, ENSULIZOLE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE

Package NDC codes

84167-828-01

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.