VALMONT DAILY VEIL MOISTURIZING FACE FLUID MINERAL SUNSCREEN SPF 30- zinc oxide gel

Valmont Daily Veil Moisturizing Face Fluid Mineral Sunscreen SPF 30 by

Drug Labeling and Warnings

Valmont Daily Veil Moisturizing Face Fluid Mineral Sunscreen SPF 30 by is a Otc medication manufactured, distributed, or labeled by CVL Cosmetics North America Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Zinc Oxide 17.5%

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 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.
• 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-sleeved shirt, pants, hats and sunglasses.
• children under 6 months of age: Ask a doctor.

Other information

Protect the product in this container from excessive heat or direct sunlight.

Inactive ingredients

C15-19 alkane, hydrogenated polydecene, squalane, water, caprylic/capric triglyceride, silica, octyldodecanol, synthetic fluorphlogopite, propanediol, ethylene/propylene/ styrene copolymer, isoamyl laurate, disteardimonium hectorite, polyhydroxystearic acid, argania spinosa kernel oil, methylsilanol mannuronate, polyglyceryl-2 oleate, tocopheryl acetate, silanediol salicylate, propylene carbonate, fragrance, ethylhexylglycerin, lecithin, isostearic acid, polyglyceryl-3 polyricinoleate, polyglyceryl-2 stearate, tocopherol, butylene/ethylene/styrene copolymer, urea, glycerin, bisabolol, potassium sorbate, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, phenoxyethanol, RNA, decarboxy carnosine HCL, butylene glycol, pentylene glycol, sodium acetylated hyaluronate, sodium hyaluronate, sodium hyaluronate crosspolymer, hydrolyzed sodium hyaluronate

Questions or comments?

1-866-411-8256

Package Labeling:

INGREDIENTS AND APPEARANCE

VALMONT DAILY VEIL MOISTURIZING FACE FLUID MINERAL SUNSCREEN SPF 30 
zinc oxide gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83883-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	175 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
C15-19 ALKANE (UNII: CI87N1IM01)
SQUALANE (UNII: GW89575KF9)
WATER (UNII: 059QF0KO0R)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
OCTYLDODECANOL (UNII: 461N1O614Y)
MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M)
PROPANEDIOL (UNII: 5965N8W85T)
ISOAMYL LAURATE (UNII: M1SLX00M3M)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
ARGAN OIL (UNII: 4V59G5UW9X)
POLYGLYCERYL-2 OLEATE (UNII: 5759J47SAM)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SILANEDIOL SALICYLATE (UNII: C054DF30K0)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ISOSTEARIC ACID (UNII: X33R8U0062)
POLYGLYCERYL-2 STEARATE (UNII: 253MC0P0YV)
TOCOPHEROL (UNII: R0ZB2556P8)
UREA (UNII: 8W8T17847W)
GLYCERIN (UNII: PDC6A3C0OX)
BISABOLOL (UNII: 24WE03BX2T)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DECARBOXY CARNOSINE HYDROCHLORIDE (UNII: 6X7K9I5QR7)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83883-001-00	1 in 1 CARTON	01/01/2026
1		5 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	01/01/2026

Labeler - CVL Cosmetics North America Inc (046869088)

Registrant - CVL Cosmetics North America Inc (046869088)