FDA.reportPublic FDA data

TotLogic Sunscreen SPF 30

Manufacturer
Logic Product Group LLC
Effective date
2019-08-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:00:10

Label at a glance#

ProductTotLogic Sunscreen SPF 30
Active ingredientZinc Oxide
Label structure11 sections

Dosage and administration

Apply liberally 15 minutes before sun exposure. Reapply: After 80 minutes of swimming or sweating. Immediately after towel drying. At least every 2 hours.

Storage and handling

Protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 20% (Non-Nano)

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

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.

Warning

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - WHEN USING SECTION

When using this product keep out of eyes.

Rinse with water to remove.

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.

STORAGE AND HANDLING SECTION

Protect this product from excessive heat and direct sun.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure.

Reapply: After 80 minutes of swimming or sweating.

Immediately after towel drying. At least every 2 hours.

Sun Protection Measures

SPL UNCLASSIFIED SECTION

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 10am - 2pm.

Wear long-sleeved shirts, pants, hats, and sunglasses.

For children under 6 months: Ask a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

DEIONIZED WATER, CAPRIC CAPRYLIC TRIGLYCERIDES (COCONUT OIL EXTRACT), GLYCERINE, HYDROGENATED CASTOR OIL SORBITAN SESQUIOLEATE, ALOE BARBADENSIS (ALOE LEAF JUICE) POLYGLYCERYL-4 ISOSTEARATE, METHYL DIHYDROABIETATE CETYL DIMETHICONE (MINERAL BASED), HEXYL LAURATE (PLANT DERIVED), SIMMONDSIA CHINENSIS (JOJOBA) HYALURONIC ACID (PLANT DERIVED) ARNICA MONTANA (ARNICA) , CAMELLIA SINENSIS (WHITE TEA) CHAMOMILLA RECUTITA (CHAMOMILE FLOWER) LAVANDULA ANGUSTIFIOLA (LAVENDER), MENTHA ARVENSIS (WILD MINT) DIMETHICONE (MINERAL BASED), MAGNESIUM SULFATE CITRUS MEDICA LIMONUM (LEMON PEEL OIL) ETHYLHEXYLGLYCERIN (PLANT DERIVED PRESERVATIVE) CITRUS BERGAMIA (BERGAMOT), PHENOXYETHANOL

Other Information

STORAGE AND HANDLING SECTION

Protect this product from excessive heat and direct sun.

PRINCIPAL DISPLAY PANEL - 89 ML Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TOTLOGIC

NATURALLY SCENTED

SUNSCREEN

MINERAL BASED
ZINC OXIDE FORMULA

SPF 30

PROVIDES UVA & UVB
PROTECTION

Water Resistant
80 Minutes

FOR FACE & BODY

PABA & PARABEN FREE
PHTHALATE FREE
BROAD SPECTRUM

PURE
GENTLE
PLANT
EXTRACTS

3 FL. OZ / 89 ML

PRINCIPAL DISPLAY PANEL - 89 ML Tube Label
PRINCIPAL DISPLAY PANEL - 89 ML Tube Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71507-001-012021-01-29C16284748780-1ba0f9c33-2845-a910-e053-dadaa90a0b85TotLogic Sunscreen SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71507-001-01TotLogic Sunscreen SPF 3089 mL in 1 TUBELOTION891

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71507-001TOTLOGIC SUNSCREEN SPF 30 (ZINC OXIDE) LOTION [LOGIC PRODUCT GROUP LLC]1Legacy NDC, 1 package rows20190830_d679c652-16be-4467-be00-efb082fbdfba.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71507-00171507-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
Zinc OxideSOI2LOH54ZACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
ALOEV5VD430YW9IACT
POLYGLYCERYL-4 ISOSTEARATE820DPX33S7IACT
METHYL DIHYDROABIETATE7666FJ0J9FIACT
HEXYL LAURATE4CG9F9W01QIACT
ARNICA MONTANAO80TY208ZWIACT
WHITE TEAO0M3396E09IACT
DIMETHICONE92RU3N3Y1OIACT
MAGNESIUM SULFATE, UNSPECIFIED FORMDE08037SABIACT
LEMON OILI9GRO824LLIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
BERGAMOT OIL39W1PKE3JIIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
ed30f2ac-0cf3-40a6-b9df-310c4bbfd960d679c652-16be-4467-be00-efb082fbdfba2019-08-29WarningsExact identifier
spl id: ed30f2ac-0cf3-40a6-b9df-310c4bbfd960
spl set id: d679c652-16be-4467-be00-efb082fbdfba

Reported adverse events (FAERS/openFDA)#

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