Sunscreen Glowing, SPF 30

Manufacturer
Cardinal Health, Inc
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:29:36

Label at a glance#

ProductSunscreen Glowing, SPF 30
Active ingredientHOMOSALATE, OCTOCRYLENE, AVOBENZONE, OCTISALATE
Label structure11 sections

Label contents#

Full prescribing information#

active ingredient

OTC - ACTIVE INGREDIENT SECTION


AVOBENZONE G63QQF2NOX 3.0%
OCTISALATE 4X49Y0596W 5.0%
OCTOCRYLENE 5A68WGF6WM 7.0%
HOMOSALATE V06SV4M95S 9%

purpose

OTC - PURPOSE SECTION

Sunscreen

WARNINGS SECTION


For external use only Do not use on damaged !i or broken skin.
When using this product keep out of eyes.Rise with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children. lf swallowed, get medical help or contact a Poison
ControlCenter right away

OTC - STOP USE SECTION

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

OTC - DO NOT USE SECTION


When using this product keep out of eyes.
Rinse with water to remove.
Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


Keep out of reach of children. lf swallowed, get medical help or contact a Poison
ControlCenter right away

INDICATIONS & USAGE SECTION


Directions
Apply liberally 15 minutes before sun exposure. Reapply: at least every 2 hours or after
80 minutes of swimming or sweating. Sun Protection Measures: $pending time in the
sun increases your risk of skin cancer andearly skin aging. To decrease this risk,
regularly use a sunscreen with a Broad Spectrum SPfof 15 or higher and other sun
protection measures including: limit time in the sun, especiallyfrom 10 a.m.-2 pm, and
wear long-sleeved shirts, pants, hats, and sunglasses. Childrenunder 6 months of age
ask a doctor.

DOSAGE & ADMINISTRATION SECTION


Apply liberally 15 minutes before sun exposure.
Reapply: at least every 2 hours or after 80 minutes of swimming or sweating.

OTC - WHEN USING SECTION


For external use only. Do not use on damagedor broken skin.
When using this product keep out of eyes.nse with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children. lf swallowed, get medical help or contact a Poison
ControlCenter right away

INACTIVE INGREDIENT SECTION

WATER
BUTYLOCTYL SALICYLATE
NEOPENTYL GLYCOL DIHEPTANOATE
MICA
CI 77891
BUTYL METHOXYDIBENZOYLMETHANE
GLYCERIN
PROPYLENE GLYCOL
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER
CETEARYL ALCOHOL
COCO-GLUCOSIDE
GLYCERYL STEARATE
PEG-100 STEARATE
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER
SILICA
POTASSIUM CETYL PHOSPHATE
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
CETEARYL ALCOHOL
HYDROXYACETOPHENONE
PHENOXYETHANOL
ETHYLHEXYLGLYCERIN
CI 77492
TRIETHOXYCAPRYLYLSILANE
DISODIUM EDTA
CI 77491
CI 77499

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70000-0280-1Sunscreen Glowing Lotion70000-0280-1Sunscreen Glowing Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70000-0280-1Sunscreen Glowing, SPF 3050 mL in 1 BOTTLELOTION503

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70000-028070000-0280-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 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
Sunscreen Glowing, SPF 30SUNSCREEN GLOWING LOTIONCardinal Health, Inc28ed3b60-1139-f657-e063-6394a90a52fa2025-12-31WarningsExact identifier
ndc (package): 70000-0280-1
ndc (product): 70000-0280
ndc11 (package): 70000028001
spl id: 473c89aa-8347-37fa-e063-6294a90afd0a
spl set id: 28ed3b60-1139-f657-e063-6394a90a52fa

Reported adverse events (FAERS/openFDA)#

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