Daily Body Moisturizer Sunscreen Broad Spectrum SPF 50

Manufacturer
Baxter Laboratories Pty. Ltd.
Effective date
2025-09-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:14:33

Label at a glance#

ProductDaily Body Moisturizer Sunscreen Broad Spectrum SPF 50
Active ingredientOCTOCRYLENE, AVOBENZONE, OCTISALATE, HOMOSALATE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Avobenzone Sunscreen

Homosalate

Octisalate

Octocrylene

OTC - PURPOSE SECTION

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.

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.

INDICATIONS & USAGE SECTION

Stop use and ask a doctor if rash occurs

WARNINGS SECTION

Warnings

For external Use Only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply liberally 15 minutes before sun exposure
  • Apply to all skin exposed to the sun
  • 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 15 or higher and other sun protection measures including:
  • Limit time in the sun, especially from 10a.m. – 2p.m.
  • Wear long-sleeve shirts, pants, hats, and sunglasses
  • Children under 6 months: Ask a doctor

INACTIVE INGREDIENT SECTION

Inactive ingredients Water, Beeswax, Cyclomethicone, Isopropyl Palmitate, Cetearyl Alcohol, Ceteareth-20, Carbomer, Sodium Stearoyl Glutamate, Tocopheryl Acetate, Benzyl Alcohol, Hydroxyacetophenone, Phenoxyethanol, Triethanolamine, Maltodextrin, Aloe Barbadensis Leaf Juice, Citric Acid

OTHER SAFETY INFORMATION

Other information

  • protect this product from excessive heat and direct sun

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Daily Body Moisturizer

SPF 50+

Non-Greasy

Sunscreen Broad Spectrum SPF50+

Water Resistant (80 Minutes)

5.0 fl. oz. (148 mL)

Daily Body SPF 50Daily Body SPF 50

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70157-029-01Daily Body Moisturizer Sunscreen Broad Spectrum SPF 50148 mL in 1 BOTTLECREAM1481
70157-029-02Daily Body Moisturizer Sunscreen Broad Spectrum SPF 501 in 1 CARTONCREAM11

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70157-02970157-029-01, 70157-029-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
Daily Body Moisturizer Sunscreen Broad Spectrum SPF 50AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEBaxter Laboratories Pty. Ltd.3e115ef1-f039-4c72-e063-6394a90a7e642025-09-05WarningsExact identifier
ndc (package): 70157-029-02
ndc (package): 70157-029-01
ndc (product): 70157-029
ndc11 (package): 70157002902
ndc11 (package): 70157002901
spl id: 3e115ef1-f03a-4c72-e063-6394a90a7e64
spl set id: 3e115ef1-f039-4c72-e063-6394a90a7e64

Reported adverse events (FAERS/openFDA)#

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