Natural Defense Foundation

Manufacturer
Baja Fur, S.A. de C.V.
Effective date
2022-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:53:06

Label at a glance#

ProductNatural Defense Foundation SPF
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE
Label structure9 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 use a water resistant sunscreen if swimming or sweating reapply at least every 2 hours children under 6 months of age: 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 ...

Storage and handling

Protect this product from excessive heat and direct sun

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.4%

Titanium Dioxide 5.8%

Zinc Oxide 1%

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

Do not use on damage or broken skin

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

Stop use and ask a doctor if rash occurs

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply liberally 15 minutes before sun exposure
use a water resistant sunscreen if swimming or sweating
reapply at least every 2 hours
children under 6 months of age: 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

Other information

STORAGE AND HANDLING SECTION

Protect this product from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water/Eau, Dimethicone, Butylene Glycol, Propanediol, Cyclopentasiloxane, Glycerin, Polymethylsilsesquioxane, Diethylhexyl Succinate, Silica, Brassica Campestris/Aleurites Fordi Oil Copolymer, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, PEG-10 Dimethicone, Calcium Aluminum Borosilicate, Methyl Methacrylate Crosspolymer, Aluminum Hydroxide, Sodium Chloride, Stearic Acid, Dimethicone/PEG-10/15 Crosspolymer, Phenoxyethanol, Caprylyl Glycol, Fragrance/Parfum, Dimethicone/Vinyl Dimethicone Crosspolymer, Ethylhexylglycerin, Hexylene Glycol, Hydrogen Dimethicone, Citric Acid, EDTA, Triethoxycaprylylsilane, PEG/PPG-18/18 Dimethicone, Dipropylene Glycol, BHT, Sodium Citrate, Tocopherol, Lecithin, Plankton Extract. May Contain/Peut Contenir: Iron Oxides (CI 77491, CI 77492, CI 77499), Mica, Titanium Dioxide (CI 77891).

Package label. PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label PDPPackage Label PDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71413-218-022023-07-28C16284748780-10191ceaa-6c7b-198a-e063-dbdaa90aec3eNatural Defense Foundation - Baja Fur

Products#

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

DailyMed product names page 1 of 1 · 40 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71413-21871413-218-01, 71413-218-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 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
e98965d5-d220-6eb9-e053-2995a90ac3f5e98965d5-d221-6eb9-e053-2995a90ac3f52022-01-01WarningsExact identifier
spl id: e98965d5-d220-6eb9-e053-2995a90ac3f5
spl set id: e98965d5-d221-6eb9-e053-2995a90ac3f5

Reported adverse events (FAERS/openFDA)#

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