HEB 50 Glow Body Oil Sunscreen

Manufacturer
H.E.B.
Effective date
2025-03-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:57:55

Label at a glance#

ProductHEB 50 Glow Body Oil Sunscreen
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure13 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

Dosage and administration

• apply liberally 15 minutes before sun exposure • hold can 4-6 inches away from body, spray evenly to ensure complete coverage • do not spray into face. Spray into hand and apply to face. • use in well ventilated, but not windy areas • reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours children under 6 months: Ask a doctor Sun Protection Measures . Spendi...

Storage and handling

• do not use near heat, flame or while smoking • avoid long term storage above 104°F (40°C)

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%, Homosalate 15.0%, Octisalate 5.0%, Octocrylene 10.0%

Purpose

OTC - PURPOSE SECTION

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

​For external use only

FLAMMABLE:

STORAGE AND HANDLING SECTION

• do not use near heat, flame or while smoking
• avoid long term storage above 104°F (40°C)

​Do not use

OTC - DO NOT USE SECTION

  • ​​on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

• keep out of eyes. Rinse with water to remove. • do not puncture or incinerate. Contents under pressure. • do not store at temperatures above 120° F.

Stop use and ask doctor

OTC - STOP USE SECTION

if ​rash occurs.

​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.

Directions

DOSAGE & ADMINISTRATION SECTION

• apply liberally 15 minutes before sun exposure
• hold can 4-6 inches away from body, spray evenly to ensure complete coverage
• do not spray into face. Spray into hand and apply to face.
• use in well ventilated, but not windy areas

• reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours

  • children under 6 months: Ask a doctor
  • 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 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

Inactive ingredients

INACTIVE INGREDIENT SECTION

CAPRYLIC/CAPRIC TRIGLYCERIDE, SD ALCOHOL 40-B, C12-15 ALKYL BENZOATE, POLYAMIDE-3, OCTYLDODECANOL, POLYESTER-8, DIISOPROPYL SEBACATE, ISODECYL NEOPENTANOATE, LAURYL LACTATE, PUNICA GRANATUM FRUIT EXTRACT, CITRUS AURANTIUM DULCIS (ORANGE) PEEL EXTRACT, CALENDULA OFFICINALIS FLOWER EXTRACT, CITRUS LIMON (LEMON) PEEL EXTRACT, CITRUS TANGERINA (TANGERINE) PEEL EXTRACT, ALARIA ESCULENTA EXTRACT, FRAGRANCE, ELAEIS GUINEENSIS (PALM) OIL, ARGANIA SPINOSA KERNEL OIL, BUTYROSPERMUM PARKII (SHEA) BUTTER, COCOS NUCIFERA (COCONUT) OIL, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, LIMNATHES ALBA (MEADOWFOAM) SEED OIL, RAPHANUS SATIVUS (RADISH) SEED OIL, VITIS VINIFERA (GRAPE) SEED OIL, TOCOPHEROL, PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE, CITRIC ACID

Other Information

SPL UNCLASSIFIED SECTION

• protect the product in this container from excessive heat and direct sun
• may stain or damage some fabrics, materials or surfaces

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HEB00365EHEB00365E

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-159-21HEB 50 Glow Body Oil Sunscreen148 mL in 1 BOTTLE, SPRAYSPRAY1481

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37808-159HEB 50 GLOW BODY OIL SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) SPRAY [H.E.B.]1Current NDC, 1 package rows20250328_31473cc9-08f5-39e3-e063-6294a90aa499.zip

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
37808-15937808-159-21

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 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
HEB 50 Glow Body Oil SunscreenAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEH.E.B.31473cc9-08f5-39e3-e063-6294a90aa4992025-03-26WarningsExact identifier
ndc (package): 37808-159-21
ndc (product): 37808-159
ndc11 (package): 37808015921
spl id: 314747d8-dc07-266e-e063-6394a90a2b0a
spl set id: 31473cc9-08f5-39e3-e063-6294a90aa499

Reported adverse events (FAERS/openFDA)#

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