FDA.reportPublic FDA data

Vigority Tallow Sunscreen SPF30

Manufacturer
FOUNDATION COMMERCE INC
Effective date
2025-08-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:11:44

Label at a glance#

ProductVigority Tallow Sunscreen SPF30
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Non-Nano Zinc Oxide 19%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

  • 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

For external use only

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

  • apply liberally 15 minutes before sun exposure
  • reapply: - after 80 minutes of swimming or sweating - immediately after towel drying - at least every 2 hours
  • 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. - 2 p.m.
  • wear long-sleeved shirts, pants, hats and sunglasses
  • children under 6 months of age: Ask a doctor

OTHER SAFETY INFORMATION

protect the product in this container from excessive heat and direct sun

INACTIVE INGREDIENT SECTION

Beef Tallow, Beeswax, Butyrospermum Parkii (Shea) Butter, Simmondsia Chinensis (Jojoba) seed oil, Cocos Nucifera (Coconut) Oil, Rubus Idaeus (Red Raspberry) Seed Oil, Daucus Carota Sativa (Carrot) Seed Oil

OTC - QUESTIONS SECTION

service@vigority.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tallow sunscreen jartallow sunscreen jar

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85739-006-01Vigority Tallow Sunscreen SPF3060 g in 1 CARTONCREAM601

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85739-00685739-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
COCOS NUCIFERA (COCONUT) OILQ9L0O73W7LIACT
BEESWAX2ZA36H0S2VIACT
BUTYROSPERMUM PARKII (SHEA) BUTTERK49155WL9YIACT
DAUCUS CAROTA SATIVA (CARROT) SEED OIL595AO13F11IACT
BEEF TALLOW98HPY76U4WIACT
ZINC OXIDESOI2LOH54ZACTIB
RUBUS IDAEUS (RASPBERRY) SEED OIL9S8867952AIACT
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL724GKU717MIACT

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
Vigority Tallow Sunscreen SPF30NON-NANO ZINC OXIDE 19%FOUNDATION COMMERCE INC3b4f5941-15ae-a760-e063-6394a90a2abe2025-08-01WarningsExact identifier
ndc (package): 85739-006-01
ndc (product): 85739-006
ndc11 (package): 85739000601
spl id: 3b4f5941-15af-a760-e063-6394a90a2abe
spl set id: 3b4f5941-15ae-a760-e063-6394a90a2abe

Reported adverse events (FAERS/openFDA)#

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