tarteguard 30 sunscreen lotion Broad Spectrum SPF 30

tarteguard 30 sunscreen Broad Spectrum SPF 30 by

Drug Labeling and Warnings

tarteguard 30 sunscreen Broad Spectrum SPF 30 by is a Otc medication manufactured, distributed, or labeled by Tarte, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

TARTEGUARD 30 SUNSCREEN BROAD SPECTRUM SPF 30- titanium dioxide and zinc oxide lotion 
Tarte, Inc.

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tarteguard 30 sunscreen lotion Broad Spectrum SPF 30

To Use

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

Warning

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

Medicinal Ingredients

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

Non-medicinal Ingredients

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.

Distr. By
tarte™, Inc. NY 10018.

PRINCIPAL DISPLAY PANEL - 7 mL Bottle Carton

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

TARTEGUARD 30 SUNSCREEN BROAD SPECTRUM SPF 30 
titanium dioxide and zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51060-330
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	33.6 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	41.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)
POLYGLYCERYL-6 DISTEARATE (UNII: Z35I17EQOP)
PROPANEDIOL (UNII: 5965N8W85T)
HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
GLYCERIN (UNII: PDC6A3C0OX)
APPLE (UNII: B423VGH5S9)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALUMINUM OXIDE (UNII: LMI26O6933)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
XANTHAN GUM (UNII: TTV12P4NEE)
TOCOPHEROL (UNII: R0ZB2556P8)
SOYBEAN OIL (UNII: 241ATL177A)
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
CHLORPHENESIN (UNII: I670DAL4SZ)
STEARIC ACID (UNII: 4ELV7Z65AP)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PASSIFLORA EDULIS SEED OIL (UNII: F3VOA31UHQ)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
GERANIOL (UNII: L837108USY)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM SALICYLATE (UNII: WIQ1H85SYP)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51060-330-01	1 in 1 CARTON	04/01/2015	11/30/2022
1		7 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	M020	04/01/2015	11/30/2022

Labeler - Tarte, Inc. (027905186)

Revised: 12/2024

Document Id: ebe06147-ba89-4dd0-b429-7676fa9f0e12

34390-5

Set id: 63a3c0d8-744c-41ea-b531-fe3ec42ee080

Version: 2

Effective Time: 20241218