FDA.reportPublic FDA data

UV Support

Manufacturer
Novamed Healthcare Private Limited
Effective date
2025-02-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:40:55

Label at a glance#

ProductUV Support
Active ingredientTITANIUM DIOXIDE, OCTOCRYLENE, HYDROXYSTEARYL ALCOHOL, BENZOPHENONE, HOMOSALATE, BUTYL METHOXYDIBENZOYLMETHANE, ETHYLHEXYL SALICYLATE
Label structure9 sections

Indications and uses

Protects against harmful UVA/UVB rays Protects from sun burn Reduces premature aging and wrinkling Prevents dry & rough skin Fills uneven skin surface Water and sweat resistant

Dosage and administration

UV-support should be used year-round before going outside. Apply UV-support to all exposed skin 15 minutes before sun exposure. Reapply UV-support after every two hours or as per need.

Label contents#

Full prescribing information#

Instructions for Use

INSTRUCTIONS FOR USE SECTION

For best results and full protection apply UV-support to all exposed skin 15 minutes before sun exposure. Reapply UV-support after every two hours or as per need.

Indications and Usage

INDICATIONS & USAGE SECTION

  • Protects against harmful UVA/UVB rays
  • Protects from sun burn
  • Reduces premature aging and wrinkling
  • Prevents dry & rough skin
  • Fills uneven skin surface
  • Water and sweat resistant

Inactive Ingredients

INACTIVE INGREDIENT SECTION

  • Acrylamide/Sodium Acryloyldimethyltaurate Copolymer
  • Caprylic/Capric Triglyceride
  • Caprylyl/Capryl Glucoside
  • Cetostearyl alcohol
  • Cetyl alcohol
  • Cyclomethicone
  • EDTA
  • Ethylene glycol distearate
  • Glycerin
  • Sodium benzoate
  • Sodium lauryl sulphate
  • Stearic acid
  • Triethanolamine
  • Water

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

  • Benzophenon
  • Butyl methoxydibenzoyl methane
  • Ethylhexyl salicylate
  • Homosalate
  • Hydroxystearyl Alcohol
  • Octocrylene
  • Titanium dioxide

Keep out of the reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of Children

Purpose

OTC - PURPOSE SECTION

Active Ingredient Purpose

Benzophenon Sunscreen (UV-A +UV-B protection)
Butyl methoxydibenzoyl methane Sunscreen (UV-A protection)
Ethylhexyl salicylate Sunscreen (UV-B protection)
Homosalate Sunscreen (UV-B protection)
Hydroxystearyl Alcohol Emulsifier
Octocrylene Sunscreen (UV-A +UV-B protection)
Titanium dioxide Opacifier + Sunscreen (UV-B protection)

Warnings

WARNINGS SECTION

  • In case of allergic reaction stop the use immediately & consult your doctor.
  • Avoid contact with eyes.
  • For external use only.
  • Keep out of the reach of children

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

UV-support should be used year-round before going outside.

Apply UV-support to all exposed skin 15 minutes before sun exposure.

Reapply UV-support after every two hours or as per need.

UV Support

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UV SupportUV Support

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84859-11584859-115-30, 84859-115-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACRYLAMIDE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (120000 MPA.S AT 1%)5F4963KLHSIACT
TRIETHANOLAMINE9O3K93S3TKIACT
SODIUM BENZOATEOJ245FE5EUIACT
GLYCERINPDC6A3C0OXIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
CETYL ALCOHOL936JST6JCNIACT
CYCLOMETHICONENMQ347994ZIACT
OCTOCRYLENE5A68WGF6WMACTIB
STEARIC ACID4ELV7Z65APIACT
HYDROXYSTEARYL ALCOHOLUN9IN5VLYEACTIB
BENZOPHENONE701M4TTV9OACTIB
HOMOSALATEV06SV4M95SACTIB
BUTYL METHOXYDIBENZOYLMETHANEG63QQF2NOXACTIB
EDTA9G34HU7RV0IACT
CAPRYLYL/CAPRYL GLUCOSIDEE00JL9G9K0IACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
WATER059QF0KO0RIACT
ETHYLHEXYL SALICYLATE4X49Y0596WACTIB
DIETHYLENE GLYCOL DISTEARATE617Q4OD69OIACT
SODIUM LAURYL SULFATE368GB5141JIACT

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
3528a1bd-dd16-fd19-e063-6294a90a76fe2f0698d0-6145-84c7-e063-6294a90af83b2025-05-15WarningsExact identifier
spl set id: 2f0698d0-6145-84c7-e063-6294a90af83b

Reported adverse events (FAERS/openFDA)#

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