SPF 50 MINERAL SUNSCREEN KIDS- zinc oxide 14.69% stick

SPF 50 Mineral Sunscreen Kids by

Drug Labeling and Warnings

SPF 50 Mineral Sunscreen Kids by is a Otc medication manufactured, distributed, or labeled by S&C Hampton Sun LLC, Inspec Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients                       Purpose

Zinc Oxide 14.69%                        Sunscreen

PURPOSE

Uses

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 liberally to cool, dry skin
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 of 15
or higher and other sun protection measures
including: limit time in the sun,especially from
10 a.m. - 2. p.m. wear a long-sleeve shirts,
pants, hats, and sunglasses. children under 6
months: Ask a doctor.

Warnings

For external use only.
Flammable:Do not use white smoking or near heat or flame.
Do not useon damaged or broken skin.
When using this product■ keep out of eyes. Rinse eyes with water
to remove.
Stop use and ask a doctor ifrash occurs.

Keep out of reach children

if swallowed, get medical
help or contact a Polson Control Center right away.

Inactive Ingredients

Butyloctyl Salicylate
Butyrospermum Parkii (Shea) Oil
C12-15 Alkyl Benzoate
Caprylic/Capric Triglyceride
Dibutyl Ethylhexanoyl Glutamide
Dibutyl Lauroyl Glutamide
Ethylhexyl Methoxycrylene
Fragrance
Octyldodecanol
Rebaudioside A
Simmondsia Chinensis (Jojoba) Seed Oil
Sodium Hyaluronate
Tocopheryl Acetate
Triethoxycaprylylsilane
Vitis Vinifera (Grape) Seed Oil
VP/Hexadecene Copolymer

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SPF 50 MINERAL SUNSCREEN KIDS 
zinc oxide 14.69% stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87170-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	14.69 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
DIBUTYL ETHYLHEXANOYL GLUTAMIDE (UNII: 0IAF2L30VS)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
FRAGRANCE LAVENDER ORC1800979 (UNII: 1B40MIN2W5)
OCTYLDODECANOL (UNII: 461N1O614Y)
REBAUDIOSIDE A (UNII: B3FUD0528F)
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
VITIS VINIFERA (GRAPE) SEED OIL (UNII: 930MLC8XGG)
VP/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87170-005-01	13 g in 1 CONTAINER; Type 0: Not a Combination Product	01/20/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/20/2025

Labeler - S&C Hampton Sun LLC (031880374)

Registrant - Inspec Solutions (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions		081030372	manufacture(87170-005)