SOLAVIDA BROAD SPECTRUM MINERAL SUNSCREEN SPF 30 - FACE- zinc oxide lotion

Solavida Broad Spectrum Mineral Sunscreen SPF 30 - Face by

Drug Labeling and Warnings

Solavida Broad Spectrum Mineral Sunscreen SPF 30 - Face by is a Otc medication manufactured, distributed, or labeled by Solavida, LLC, Columbia Cosmetics Manufacturing, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Zinc Oxide 22.6

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

on damaged or broken skin.

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a physician 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: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours

- 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 including: limiting time in the sun, especially from 10 a.m. - 2 p.m. wearing long sleeve shirts, pants, hats, and sunglasses.

Other information

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

- May stain some fabrics

Inactive ingredients

Water (Aqua), Caprylyl Caprylate/Caprate, Dicaprylyl Carbonate, Polyglyceryl-2 Oleate, Polyhydroxystearic Acid, Glycerin, Hydrogenated Methyl Abietate, Cetyl Alcohol, Niacinamide, Lactic Acid, Triethoxycaprylylsilane, Polyglyceryl-2 Stearate, Microcrystalline Cellulose, Sodium Hyaluronate, Ethyl Macadamiate, Cellulose Gum, Phytic Acid, Xanthan Gum, Chamomilla Recutita (Matricaria) Flower Extract*, Tocopheryl Acetate, Ceramide NP, Ceramide AP, Ceramide EOP, Phytosphingosine, Cholesterol (Vegan), Ethylhexylglycerin, Sodium Lauroyl Lactylate, Phenoxyethanol, Carbomer, Glyceryl Caprylate, Caprylhydroxamic Acid.

Questions or Comments?

Call 1-877-SOLAVIDA

Principal Display Panel

SPF
30
FACE

SOLAVIDA™

WATER RESISTANT
(80 MINUTES)

BROAD SPECTRUM
MINERAL SUNSCREEN

1.75 FL OZ / 50 ML

INGREDIENTS AND APPEARANCE

SOLAVIDA BROAD SPECTRUM MINERAL SUNSCREEN SPF 30 - FACE 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87422-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	22.6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
CERAMIDE AP (UNII: F1X8L2B00J)
CAPRYLYL CAPRYLATE/CAPRATE (UNII: 22MCG4RSMR)
HYDROGENATED METHYL ABIETATE (UNII: A23O709X8O)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
CERAMIDE 1 (UNII: 5THT33P7X7)
GLYCERIN (UNII: PDC6A3C0OX)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
POLYGLYCERYL-2 OLEATE (UNII: 5759J47SAM)
XANTHAN GUM (UNII: TTV12P4NEE)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
NIACINAMIDE (UNII: 25X51I8RD4)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
POLYGLYCERYL-2 STEARATE (UNII: 253MC0P0YV)
CELLULOSE GUM (UNII: K679OBS311)
ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
CARBOMER (UNII: 0A5MM307FC)
MATRICARIA CHAMOMILLA FLOWERING TOP (UNII: 3VNC7T6Z02)
CHOLESTEROL (UNII: 97C5T2UQ7J)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
PHYTIC ACID (UNII: 7IGF0S7R8I)
LACTIC ACID (UNII: 33X04XA5AT)
CERAMIDE NP (UNII: 4370DF050B)
CETYL ALCOHOL (UNII: 936JST6JCN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87422-001-01	1 in 1 CARTON	02/09/2026
1		50 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	02/09/2026

Labeler - Solavida, LLC (134927687)

Establishment
Name	Address	ID/FEI	Business Operations
Columbia Cosmetics Manufacturing, Inc.		068267863	manufacture(87422-001)