SEPHORA DAILY SUNSCREEN CREAM BROAD SPECTRUM SPF 30- zinc oxide cream

Sephora Daily Sunscreen Cream Broad Spectrum SPF 30 by

Drug Labeling and Warnings

Sephora Daily Sunscreen Cream Broad Spectrum SPF 30 by is a Otc medication manufactured, distributed, or labeled by S+. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Zinc Oxide 15.5%

Purpose

Sunscreen

Uses

• Helps prevent sunburn.
• If used as directed with other sun protection measures (see Directions), decreses the risk of skin cancer and early skin aging caused by the sun

Warnings

For external use only

Do not use

• on damaged 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

• Apply liberally 15 minutes before sun exposure
• Reapply at least every 2 hours 
• Use a water resistant sunscreen if swimming or sweating
• Children under 6 months: 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 incluing:
• limit time in the sun, especialy from 10 a.m. - 2 p.m.
• wear long-sleeved shirts, pants, hats, and sunglasses

Other information

• Protect the product in this container from excessive heat and direct sun

Inactive ingredients

Water (Aqua), C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Butyloctyl Salicylate, Dimethicone, Glycerin, Ethylhexyl Palmitate, Propanediol, Shea Butter (Butyrospermum Parkii), Safflower (Carthamus Tinctorius) Oleosomes, Glyceryl Stearate Se, Polyhydroxystearic Acid, Sorbitan Isostearate, Cetyl Alcohol, Pentaerythrityl Tetraisostearate, Phenyl Trimethicone, Silica, Inulin Lauryl Carbamate, Ethylhexylglycerin, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Phenoxyethanol, Hydroxyacetophenone, Polysilicone-11, Xanthan Gum, Gluconolactone, Trisodium Ethylenediamine Disuccinate, Sodium Citrate, Sodium Benzoate, Tocopherol, Citric Acid.

Package Labeling:

INGREDIENTS AND APPEARANCE

SEPHORA DAILY SUNSCREEN CREAM BROAD SPECTRUM SPF 30 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 31720-251
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	155 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
PROPANEDIOL (UNII: 5965N8W85T)
SHEA BUTTER (UNII: K49155WL9Y)
CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
CETYL ALCOHOL (UNII: 936JST6JCN)
PENTAERYTHRITYL TETRAISOSTEARATE (UNII: 9D7IK5483F)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
INULIN LAURYL CARBAMATE (UNII: 48RFF58ESG)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
XANTHAN GUM (UNII: TTV12P4NEE)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM BENZOATE (UNII: OJ245FE5EU)
TOCOPHEROL (UNII: R0ZB2556P8)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 31720-251-06	1 in 1 BOX	04/10/2025
1		10 mL in 1 TUBE; 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	04/10/2025

Labeler - S+ (572406531)

Registrant - S+ (572406531)