tarteguard 30 sunscreen lotion Broad Spectrum SPF 30

Label at a glance#

Label contents#

Full prescribing information#

To Use

INDICATIONS & USAGE SECTION

Provides daily hydration & helps protect skin from UVA/UVB rays. Apply prior to sun exposure.

Warning

WARNINGS SECTION

OTC - DO NOT USE SECTION

Discontinue use if skin irritation develops or increases. If irritation persists, consult a health care practitioner. Avoid contact with eyes.

OTC - ACTIVE INGREDIENT SECTION

Medicinal Ingredients

OTC - PURPOSE SECTION

Zinc Oxide 4.13% w/w, Titanium Dioxide 3.36% w/w

Non-medicinal Ingredients

INACTIVE INGREDIENT SECTION

Eau, butyloctyl salicylate, coco-caprylate/-caprate, C12-15 alkyl benzoate, caprylic/capric triglyceride, diheptyl succinate, polyglyceryl-6 distearate, propanediol, jojoba esters, glycerin, pyrus malus (apple) fruit extract, polysorbate 20, polyhydroxystearic acid, polymethylsilsesquioxane, potassium cetyl phosphate, phenoxyethanol, alumina, diethylhexyl syringylidenemalonate, xanthan gum, tocopherols, glycine soja (soybean) oil, capryloyl glycerin/sebacic acid copolymer, citric acid, triethoxycaprylylsilane, lonicera caprifolium (honeysuckle) flower extract, trisodium ethylenediamine disuccinate, chlorphenesin, fragrance/parfum, stearic acid, ethylhexylglycerin, passiflora edulis seed oil, lonicera japonica (honeysuckle) flower extract, algae extract, pseudoalteromonas exopolysaccharides, sodium hyaluronate, sodium salicylate, propylene glycol, sodium dehydroacetate.

SPL UNCLASSIFIED SECTION

Distr. By
tarte™, Inc. NY 10018.

PRINCIPAL DISPLAY PANEL - 7 mL Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tarte
high-performance naturals™

TARTEGUARD
30

moisturizing sunscreen lotion
Broad Spectrum UVA/UVB Protection
SPF 30 / FPS 30

7 mL / 0.23 Fl. Oz

NPN 8005 6077

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 2 · 41 matching rows.

• tarteguard 30 sunscreen Broad Spectrum SPF 30
• Titanium Dioxide and Zinc Oxide
• TITANIUM DIOXIDE
• ZINC OXIDE
• WATER
• BUTYLOCTYL SALICYLATE
• COCOYL CAPRYLOCAPRATE
• ALKYL (C12-15) BENZOATE
• MEDIUM-CHAIN TRIGLYCERIDES
• DIHEPTYL SUCCINATE
• POLYGLYCERYL-6 DISTEARATE
• PROPANEDIOL
• HYDROGENATED JOJOBA OIL, RANDOMIZED
• GLYCERIN
• APPLE
• POLYSORBATE 20
• POLYHYDROXYSTEARIC ACID (2300 MW)
• POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)
• POTASSIUM CETYL PHOSPHATE
• PHENOXYETHANOL
• ALUMINUM OXIDE
• DIETHYLHEXYL SYRINGYLIDENEMALONATE
• XANTHAN GUM
• TOCOPHEROL
• SOYBEAN OIL
• CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)
• CITRIC ACID MONOHYDRATE
• TRIETHOXYCAPRYLYLSILANE
• LONICERA CAPRIFOLIUM FLOWER
• TRISODIUM ETHYLENEDIAMINE DISUCCINATE
• CHLORPHENESIN
• STEARIC ACID
• ETHYLHEXYLGLYCERIN
• PASSIFLORA EDULIS SEED OIL
• LINALOOL, (+/-)-
• BUTYLPHENYL METHYLPROPIONAL
• GERANIOL
• HYALURONATE SODIUM
• SODIUM SALICYLATE
• PROPYLENE GLYCOL

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 39 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.

Reported adverse events (FAERS/openFDA)#

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