EUCERIN SENSITIVE MINERAL SPF 50 SUNSCREEN- zinc oxide lotion

Eucerin Sensitive Mineral SPF 50 Sunscreen by

Drug Labeling and Warnings

Eucerin Sensitive Mineral SPF 50 Sunscreen by is a Otc medication manufactured, distributed, or labeled by Beiersdorf Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Zinc Oxide

Purpose

Sunscreen

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

Warnings

For external use only

DO NOT USE

Do not useon damaged or broken skin

WHEN USING

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

STOP USE

Stop use and ask a doctor ifrash occures

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

■ 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.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-sleeve shirts, pants, hats, and sunglasses

■ children under 6 months: Ask a doctor

Other information

■ protect this product from excessive heat and direct sun

■ may stain or damage some fabrics or surfaces

Inactive ingredients

Water, C12-15 Alkyl Benzoate, Isopropyl Palmitate, Butyloctyl Salicylate, Ethylhexyl Pelargonate, Cetyl PEG/PPG-10/1
Dimethicone, Propylene Glycol, Cyclopentasiloxane, Bis-Octyldodecyl Dimer Dilinoleate/Propanediol Copolymer, Dimethicone, Diethylhexyl Syringylidenemalonate, Ethylhexyl Methoxycrylene, Polyester-27, Glycyrrhetinic Acid, Glycyrrhiza Inflata Root Extract, Tocopherol (Vitamin E), Sodium Ascorbyl Phosphate, Beeswax, Hydroxyacetophenone, Caprylyl Glycol, 1,2-Hexanediol,
PEG-12 Dimethicone Crosspolymer, Triethoxycaprylylsilane, Sodium Chloride

Questions?

1-800-227-4703

PRINCIPAL DISPLAY PANEL

Eucerin ®

Sensitive Mineral

Zinc Oxide Protection

Lightweight Sunscreen Lotion

50 Broad Spectrum SPF 50

Hypoallergenic | Fragrance Free

No Oxybenzone and Octinoxate

5 AOX Shield Antioxidant Defense

Developed With Dermatologists

Water Resistant (80 Minutes)

4 FL OZ (118 mL)

INGREDIENTS AND APPEARANCE

EUCERIN SENSITIVE MINERAL SPF 50 SUNSCREEN 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66800-1000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	24 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
TOCOPHEROL (UNII: R0ZB2556P8)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYESTER-7 (UNII: 0841698D2F)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)
BIS-OCTYLDODECYL DIMER DILINOLEATE/PROPANEDIOL COPOLYMER (UNII: TY3J98ZR7R)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
WATER (UNII: 059QF0KO0R)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ETHYLHEXYL PELARGONATE (UNII: 3YU1SQ04DV)
GLYCYRRHIZA INFLATA ROOT (UNII: 1MV1Z7MKVQ)
GLYCYRRHETINIC ACID (UNII: P540XA09DR)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)

Product Characteristics
Color	white (off-white to yellow)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66800-1000-1	118 g in 1 TUBE; Type 0: Not a Combination Product	11/03/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/03/2021

Labeler - Beiersdorf Inc (001177906)