LIGHT AND DELICATE SUNSCREEN SPF15

Manufacturer
Genuine Virgin Aloe Corporation
Effective date
2019-05-28
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-02 00:23:29

Label at a glance#

ProductLIGHT AND DELICATE SUNSCREEN SPF15
Active ingredientAVOBENZONE, OXYBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT

  • AVOBENZONE 3%
  • BENZOPHENONE-3  5%
  • HOMOSALATE  5%
  • OCTINOXATE  7.49%
  • OCTISALATE  5%
  • OCTOCRYLENE  2.7%

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS

  •  FOR DAILY USE, ALLOW PRODUCT TO ABSORB COMPLETELY BEFORE APPLYING MAKE-UP
  •  APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE
  •  REAPPLY AS NEEDED OR AFTER TOWEL DRYING, SWIMMING, OR PERSPIRING
  •  SUN PROTECTION MEASURES
  •  SPEDNING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY
  •  AGEING. TO DECREASE THIS RISK, REGULARLY USE A SUNSCREEN WITH A BROAD
  •  SPECTRUM SPF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUDING
  •  LIMITING TIME IN THE SUN, ESPECIALLY FROM 10 AM TO 2 PM.
  •  WEAR LONG SLEEVE SHIRTS, PANTS, HATS AND SUNGLASSES
  •  FOR USE ON CHILDREN 6 MONTHS AND OLDER/ CHILDREN UNDER 6 MONTHS ASK A DOCTOR

OTC - PURPOSE SECTION

PURPOSE:

  • SUNSCREEN

INDICATIONS & USAGE SECTION

Uses:

  • DAILY MOISTURIZER
  • HELPS 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.

WARNINGS SECTION

WARNINGS

FOR EXTERNAL USE ONLY

OTC - WHEN USING SECTION

WHEN USING THIS PRODUCT

  • KEEP OUT OF THE EYES.
  • RINSE WITH WATER TO REMOVE

OTC - STOP USE SECTION

STOP USE AND ASK A DOCTOR IF

  • IF RASH OR IRRITATION DEVELOPS AND LASTS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

  • IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

INACTIVE INGREDIENT SECTION

Inactive ingredients: ALARIA ESCULENTA EXTRACT, BEHENYL ALCOHOL, BETAINE, C12-15 ALKYL BENZOATE,

CAPRYLIC/CAPRIC TRIGLYCERIDE, CETYL ALCOHOL, DIISOPROPYL SEBACATE, DISODIUM EDTA, GLUCONO LACTONE,

GLYCERIN, GLYCERYL STEARATE, LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE, LONICERA CAPRIFOLIUM (HONEYSUCKLE)

FLOWER EXTRACT, LONICERA JAPONMICA (HONEYSUCKLE) FLOWER EXTRACT, PANTHENOL, POPULUS TREMULOIDES BARK EXTRACT,

POTASSIUM CETYL PHOSPHATE, POTASSIUM SORBATE, SODIUM HYALURONATE, TOCOPEROL, WATER(AQUA), XANTHAN GUM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FINAL Triderma_SPF_FDA_LabelFINAL Triderma_SPF_FDA_Label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10738-01410738-014-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 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
b9f9a39f-46b7-612b-e053-2995a90aac397c7e29f6-577a-44f4-9f4f-cfb9cd3b336a2021-01-28WarningsExact identifier
spl set id: 7c7e29f6-577a-44f4-9f4f-cfb9cd3b336a

Reported adverse events (FAERS/openFDA)#

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