YENSA BC FOUNDATION

Manufacturer
YENSA LLC
Effective date
2024-01-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:14:25

Label at a glance#

ProductYENSA BC FOUNDATION SPF 40
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE
Label structure9 sections

Dosage and administration

FOR SUNSCREEN USE: APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE. REAPPLY AT LEAST EVERY 2 HOURS. USE A WATER RESISTANT SUNSCREEN IF SWIMMING OR SWEATING. SUN PROTECTION MEASURES: SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY SKIN AGING. TO DECREASE THIS RISK, REGULARLY USE A SUNSCREEN WITH A BROAD SPECTRUM SPF VALUE OF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUDING:    LIMIT TIM...

Storage and handling

PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN LIGHT.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

OCTINOXATE 7.4%

TITANIUM DIOXIDE 9.4%

ZINC OXIDE 7.0%

Purpose

OTC - PURPOSE SECTION

SUNSCREEN

Use

INDICATIONS & USAGE SECTION

USE HELPS PREVENT SUNBURN

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

DO NOT USE ON DAMAGED OR BROKEN SKIN.

WHEN USING THIS PRODUCTKEEP OUT OF EYES. RINSE WITH WATER TO REMOVE.

STOP USE AND ASK A DOCTOR IF RASH OCCURS

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.

Directions

DOSAGE & ADMINISTRATION SECTION

FOR SUNSCREEN USE:

  • APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.
  • REAPPLY AT LEAST EVERY 2 HOURS.
  • USE A WATER RESISTANT SUNSCREEN IF SWIMMING OR SWEATING.

SUN PROTECTION MEASURES:

  • SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY SKIN AGING. TO DECREASE THIS RISK, REGULARLY USE A SUNSCREEN WITH A BROAD SPECTRUM SPF VALUE OF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUDING:
  •    LIMIT TIME IN THE SUN, ESPECIALLY FROM 10 A.M. TO 2 P.M.
  •    WEAR LONG-SLEEVED SHIRTS, PANTS, HATS AND SUNGLASSES
  • CHILDREN UNDER 6 MONTHS OF AGE: ASK A DOCTOR

Other information

STORAGE AND HANDLING SECTION

PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN LIGHT.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, CYCLOPENTASILOXANE, CYCLOHEXASILOXANE, CAPRYLIC/CAPRIC TRIGLYCERIDE, BUTYLENE GLYCOL, CETYL PEG/PPG-10/1 DIMETHICONE, SORBITAN SESQUIOLEATE, ETHYLHEXYL PALMITATE, ARBUTIN, DIMETHICONE, SODIUM CHLORIDE, BEESWAX, STEARALKONIUM HECTORITE, MAGNESIUM ALUMINUM SILICATE, PHENOXYETHANOL, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, OZOKERITE, PEG-10 DIMETHICONE CROSSPOLYMER, ARONIA MELANOCARPA FRUIT EXTRACT, SESAMUM INDICUM (SESAME) SEED EXTRACT, NIGELLA SATIVA SEED EXTRACT, RUBUS FRUTICOSUS (BLACKBERRY) FRUIT EXTRACT, ORYZA SATIVA (RICE) EXTRACT, UNDARIA PINNATIFIDA EXTRACT, LAMINARIA JAPONICA EXTRACT, CAMELIA SINENSIS LEAF EXTRACT, ADENOSINE, OLEA EUROPAEA (OLIVE) FRUIT OIL, CITRUS AURANTIUM BERGAMIA (BERGAMOT) FRUIT OIL, SESAMUM INDICUM (SESAME) SEED OIL, LENTINUS EDODES EXTRACT, URTICA DIOICA (NETTLE) EXTRACT, SALVIA HISPANICA SEED EXTRACT, LAVENDULA ANGUSTIFOLIA (LAVENDER) OIL, CANAGA ODORATA FLOWER OIL, PELARGONIUM GRAVEOLENS FLOWER OIL, CITRUS AURANTIUM DULCIS (ORANGE) OIL, CYMBOPOGON MARTINI OIL, MICHELIA ALBA FLOWER OIL, EUGENIA CARYOPHYLLUS (CLOVE) LEAF OIL, EUCALYPTUS GLOBULUS LEAF OIL, 1,2-HEXANEDIOL, JASMINUM OFFICINALE (JASMINE) OIL, SODIUM HYALURONATE, ETHYLHEXYLGLYCERIN, ACETYL HEXAPEPTIDE-8, LINALOOL, LIMONENE

MAY CONTAIN:  IRON OXIDES (CI 77491/77492/77499)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b UC_BC Foundation_Fair01b UC_BC Foundation_Fair

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72782-101YENSA BC FOUNDATION SPF 40 (OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE) CREAM [YENSA LLC]3Legacy NDC20240116_fe908bcb-7ae6-497f-b917-b6e6eef83fb9.zip

Products#

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

DailyMed product names page 1 of 2 · 57 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72782-10172782-101-32, 72782-101-10

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 54 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
474a1f26-1fa8-6ff5-e063-6394a90a94d2fe908bcb-7ae6-497f-b917-b6e6eef83fb92025-12-31WarningsExact identifier
spl set id: fe908bcb-7ae6-497f-b917-b6e6eef83fb9

Reported adverse events (FAERS/openFDA)#

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