Resting Beach Face Broad Spectrum SPF 30 Sunscreen Serum

Manufacturer
Baxter Laboratories Pty. Ltd.
Effective date
2025-09-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:15:05

Label at a glance#

ProductResting Beach Face Broad Spectrum SPF 30 Sunscreen Serum
Active ingredientOCTISALATE, HOMOSALATE, AVOBENZONE, OCTOCRYLENE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purpose

Avobenzone 3%....Sunscreen

Homosalate 8%.....Sunscreen

Octisalate 4%......Sunscreen

Octocrylene 2%...Sunscreen

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 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
  • 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 sub 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: Ask a doctor

INACTIVE INGREDIENT SECTION

water, cyclomethicone, isostearyl neopentanoate, glycerin, ceteareth-20, cetearyl alcohol, sodium hyaluronate, spinacia oleracea leaf extract, alteromonas ferment extract, camellia sinensis leaf extract, caprylyl glycol, saccharide isomerate, xanthan gum, PEG-40 stearate, triacontanyl PVP, silica, ammonium acryloyldimethyltaurate/vp copolymer, butylene glycol, cetyl dimethicone, caprylhydroxamic acid, disodium EDTA, fragrance, tocopheryl acetate, helianthus annuus (sunflower) seed oil, triethanolamine, citric acid, sodium citrate, potassium sorbate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Everyday Humans

Resting Beach face

SPF 30

Sun-screen Serum

Spinach

Green Tea

Hyaluronic Acid

I'm a sheer + hydrating SPF

Broad Spectrum SPF 30

Dermatologically testing

1.7 FL. OZ- 50ML

Resting Beach Face SPF 30Resting Beach Face SPF 30

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70157-031-01Resting Beach Face Broad Spectrum SPF 30 Sunscreen Serum50 mL in 1 TUBECREAM501

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70157-03170157-031-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 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
Resting Beach Face Broad Spectrum SPF 30 Sunscreen SerumAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEBaxter Laboratories Pty. Ltd.3e8b0a0b-846a-cce7-e063-6294a90a6bb32025-09-11WarningsExact identifier
ndc (package): 70157-031-01
ndc (product): 70157-031
ndc11 (package): 70157003101
spl id: 3e8b0a0b-846b-cce7-e063-6294a90a6bb3
spl set id: 3e8b0a0b-846a-cce7-e063-6294a90a6bb3

Reported adverse events (FAERS/openFDA)#

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