SPF 50 Broad Spectrum Sunscreen Lotion

Manufacturer
SnugZ/USA, LLC
Effective date
2025-12-29
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:29:26

Label at a glance#

ProductSnugZ SPF 50 Broad Spectrum Sunscreen
Active ingredientOCTOCRYLENE, AVOBENZONE, OCTINOXATE, OCTISALATE
Label structure1 sections

Label contents#

Full prescribing information#

SPF 50 Broadspectrum Sunscreen Lotion

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZSUNPL10-UNSCZSUNPL10-UNSC

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76309-551-01SnugZ SPF 50 Broad Spectrum Sunscreen28 mL in 1 BOTTLELOTION286
76309-551-02SnugZ SPF 50 Broad Spectrum Sunscreen56 mL in 1 BOTTLELOTION566
76309-551-04SnugZ SPF 50 Broad Spectrum Sunscreen112 mL in 1 BOTTLELOTION1126
76309-551-08SnugZ SPF 50 Broad Spectrum Sunscreen226 mL in 1 BOTTLELOTION2266
76309-551-19SnugZ SPF 50 Broad Spectrum Sunscreen56 mL in 1 BOTTLELOTION566
76309-551-51SnugZ SPF 50 Broad Spectrum Sunscreen30 mL in 1 TUBELOTION306
76309-551-61SnugZ SPF 50 Broad Spectrum Sunscreen39.75 mL in 1 POUCHLOTION39.756
76309-551-62SnugZ SPF 50 Broad Spectrum Sunscreen85.17 mL in 1 POUCHLOTION85.176

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
SnugZ SPF 50 Broad Spectrum SunscreenSPF 50 BROAD SPECTRUM SUNSCREENSnugZ/USA, LLCb7a3eed5-c8ca-ffda-e053-2a95a90a73bb2025-12-29WarningsExact identifier
ndc (package): 76309-551-62
ndc (package): 76309-551-08
ndc (package): 76309-551-51
ndc (package): 76309-551-01
ndc (package): 76309-551-19
ndc (package): 76309-551-04
ndc (package): 76309-551-61
ndc (package): 76309-551-02
ndc (product): 76309-551
ndc11 (package): 76309055102
ndc11 (package): 76309055101
ndc11 (package): 76309055104
ndc11 (package): 76309055161
ndc11 (package): 76309055119
ndc11 (package): 76309055162
ndc11 (package): 76309055108
ndc11 (package): 76309055151
spl id: 47209cb5-cb4e-d22d-e063-6394a90a834d
spl set id: b7a3eed5-c8ca-ffda-e053-2a95a90a73bb

Reported adverse events (FAERS/openFDA)#

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