FDA.reportPublic FDA data

Active Ingredients

Manufacturer
MIXIK, INC.
Effective date
2026-07-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
weekly-update
Hydrated at
2026-07-17 21:44:08

Label at a glance#

ProductSunny C Sunscreen SPF 50
Active ingredientOCTISALATE, AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENE
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Homosalate (7%), Octinoxate (7%), Octisalate (4%), Avobenzone (3%), Octocrylen (3%)

Purpose

Sunscreen Secondary PkgSecondary Pkg

DOSAGE & ADMINISTRATION SECTION

Apply generously 15 minutes before sun exposure.

Warnings

WARNINGS SECTION

For External Use only.

Do not use on damaged on broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If product swallowed, get medical help or contact a Poison Control Center.

INACTIVE INGREDIENT SECTION

Water, Alcohol Denat.,Ethylhexyl Methoxycrylene, Pentylene Glycol, Butylene Glycol, Butyloctyl Salicylate,
Styrene/Acrylates Copolymer, Poly C10-30 Alkyl Acrylate, Sodium Polyacrylate, VP/Eicosene Copolymer, PEG-2 Stearate, Glycol Stearate, Triceteareth-4 Phosphate,
Phenoxyethanol, Ethylhexyl Stearate, Ammonium Acryloyldimethyltaurate/VP Copolymer, Allantoin, Tocopheryl Acetate, Trideceth-6, Disodium EDTA, C11-13 Isoalkane,
Xanthan Gum, Sodium Hyaluronate, BHT, Ammonium Hydroxide, Persea Gratissima (Avocado) Oil, 3-O-Ethyl Ascorbic Acid, Ethylhexylglycerin, 1,2-Hexanediol, Agave
Tequilana Leaf Extract, Caprylyl Glycol, Niacinamide, Glycerin, Caprylhydroxamic Acid, Retinyl Palmitate, Riboflavin, Biotin, Ascorbic Acid, Carnitine HCl, Tocopherol,
Thiamine HCl, Pantothenic Acid, Folic Acid

INDICATIONS & USAGE SECTION

Uses

- Helps prevent sunburn

- if used as directed with other sunprotection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings

Keep out of reach of children. If product swallowed, get medical help or contact a Poison Control Center.

OTC - PURPOSE SECTION

Active Ingredients

Homosalate (7%), Octinoxate (7%), Octisalate (4%), Avobenzone (3%), Octocrylene (3%)

Purpose

Sunscreen

Sunny C Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SPF 50

Sunny C Sunscreen

Broad Spectrum SPF 50+

PA+++

Refreshing, lightweight sunscreen for UVA & UVB protection

50ml/1.69 fl. oz.

MIXIK

Principal PanelPrincipal Panel

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87611-324587611-3245-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
PENTYLENE GLYCOL50C1307PZGIACT
OCTINOXATE4Y5P7MUD51ACTIB
OCTOCRYLENE5A68WGF6WMACTIB

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
Sunny C Sunscreen SPF 50SUNNY C SUNSCREENMIXIK, INC.4ed2a482-6c63-69f5-e063-6394a90ad3ee2026-07-08WarningsExact identifier
ndc (package): 87611-3245-1
ndc (product): 87611-3245
ndc11 (package): 87611324501
spl id: 561c2d21-b1a2-fb89-e063-6394a90a589c
spl set id: 4ed2a482-6c63-69f5-e063-6394a90ad3ee

Reported adverse events (FAERS/openFDA)#

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