Protective Day Lotion

Manufacturer
USANA Health Sciences, Inc.
Effective date
2026-03-11
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
monthly-update
Hydrated at
2026-06-03 17:58:41

Label at a glance#

ProductProtective Day
Active ingredientAVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENE
Label structure9 sections

Indications and uses

• 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.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3% Homosalate 10% Octinoxate 7.5% Octocrylene 2%


Purpose

OTC - PURPOSE SECTION

Sunscreen Sunscreen Sunscreen Sunscreen


Uses

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

WARNINGS SECTION

• on damaged or broken skin. • keep out of eyes. Rinse with water to remove. • rash occurs. For External use only. Do not use When using this product Stop use and ask a doctor if


Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

• Shake well and apply a pearl-sized amount to face and neck • Apply generously and evenly 15 minutes before sun exposure • Reapply at least every 2 hours • Use a water resistant sunscreen if swimming or sweating • . 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




Sun Protection Measures

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Isopropyl Lauroyl Sarcosinate, Pentylene Glycol, Mica, Ethylhexyl Palmitate, Cetearyl Alcohol, Dimethicone, Polysorbate 60, Ocimum Basilicum Hairy Root Culture Extract, Glycine Soja (Soybean) Seed Extract, Olea Europaea (Olive) Fruit Extract, Citrullus Lanatus (Watermelon) Fruit Extract, Lens Esculenta (Lentil) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Acanthopanax Senticosus (Eleuthero) Root Extract, Panax Ginseng Root Extract, Panax Quinquefolius Root Extract, Butyrospermum Parkii (Shea) Butter, Rosa Multiflora Fruit Extract, Ceramide NP, Sodium PCA,Glycerin, Sodium Lactate, Ceteth-10 Phosphate, Dicetyl Phosphate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Carbomer, Silica, Hydrolyzed Corn Starch, Citric Acid, Potassium Hydroxide, Fragrance.























Other Information

SPL UNCLASSIFIED SECTION

• Protect the product in this container from excessive heat and direct sun

Questions or Comments?

OTC - QUESTIONS SECTION

Call toll free 1-800-950-9595

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Protective Day LotionProtective Day Lotion

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51861-060-002023-02-17C16284748780-1f386c649-e4af-0266-e053-dadaa90a7c1aProtective Day Lotion
51861-060-002023-01-30C16284748780-1f386c649-e4af-0266-e053-dadaa90a7c1aProtective Day Lotion

Products#

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

DailyMed product names page 1 of 1 · 36 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51861-06051861-060-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 34 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
4cb8c2ba-aff3-3efb-e063-6294a90a65ae401e53ee-d69d-4ba6-8cbd-8ebfbf6c606e2026-03-11WarningsExact identifier
spl id: 4cb8c2ba-aff3-3efb-e063-6294a90a65ae
spl set id: 401e53ee-d69d-4ba6-8cbd-8ebfbf6c606e

Reported adverse events (FAERS/openFDA)#

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