ZINC OXIDE 20%- sunscreen spf 50 mineral lotion

Zinc Oxide 20% by

Drug Labeling and Warnings

Zinc Oxide 20% by is a Otc medication manufactured, distributed, or labeled by S&C Hampton Sun, Inspec Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient                                                        Purpose Zinc Oxide 20% .......................................................Sunscreen

PURPOSE

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.

Directions

Apply evenly to face and neck 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
10a.m.– 2p.m. . Wear long-sleeve shirts, pants, hats, and sunglasses.
. Children under 6 months: Ask a doctor.

Warnings For external use only.

Do not useon damaged or broken skin.
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor ifrash occurs.

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center right away

Inactive ingredients

Aloe Barbadensis Leaf Juice
Ascorbyl Tetraisopalmitate
Butylene Glycol
Butyloctyl Salicylate
Caprylic/Capric Triglyceride
Carbomer
Ceramide AP
Ceramide EOP
Ceramide NP
Cetearyl Olivate
Cholesterol
Citric Acid
Dicaprylyl Carbonate
Dimethicone
Ethylhexyl Methoxycrylene
Ethylhexylglycerin
Fragrance
Helianthus Annuus (Sunflower) Seed Oil
Hydrogenated Castor Oil
Isopropyl Myristate
Magnesium Sulfate
Niacinamide
Persea Gratissima
Phenoxyethanol
Phytosphingosine
Polyglyceryl-3 Polyricinoleate
Polyhydroxystearic Acid
Potassium Sorbate
Propylene Glycol
Sodium Benzoate
Sodium Hyaluronate
Sodium Lauroyl Lactylate
Sorbitan Oleate
Sorbitan Olivate
Synthetic Beeswax
Tocopheryl Acetate
VP/Hexadecene Copolymer
Water
Xanthan Gum

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZINC OXIDE 20% 
sunscreen spf 50 mineral lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87170-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	20 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CARBOMER (UNII: 0A5MM307FC)
CERAMIDE AP (UNII: F1X8L2B00J)
CERAMIDE 9 (UNII: 88KCS7120E)
CERAMIDE NP (UNII: 4370DF050B)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
CHOLESTEROL (UNII: 97C5T2UQ7J)
CITRIC ACID (UNII: 2968PHW8QP)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
DIMETHICONE (UNII: 92RU3N3Y1O)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI)
CASTOR OIL (UNII: D5340Y2I9G)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
NIACINAMIDE (UNII: 25X51I8RD4)
PERSEA GRATISSIMA (AVOCADO) OIL (UNII: 6VNO72PFC1)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
SORBITAN OLEATE (UNII: 06XEA2VD56)
SORBITAN OLIVATE (UNII: MDL271E3GR)
SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
VP/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87170-006-10	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/09/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/09/2025

Labeler - S&C Hampton Sun (031880374)

Registrant - Inspec Solutions (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions		081030372	manufacture(87170-006)