BOB KIDS SPF 30 ZINC ONLY- zinc oxide powder

BOB KIDS SPF 30 Zinc only by

Drug Labeling and Warnings

BOB KIDS SPF 30 Zinc only by is a Otc medication manufactured, distributed, or labeled by SPF Ventures, LLC, Innovation Labs, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Zinc Oxide 22.1%

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

Do not use on damaged or broken skin.

When using thi sproduct

When using this product keeo out of eyes. Rinse with water to remove.

Stop use and ask a doctor

Stop use and ask a doctor if rash occurs.

Keep out of reach of children

If product is 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
• Sun Proection Measures: Spending time in the sun increases yur 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 10am-2pm; Wear long-sleeved shirts, pants, hats and sunglasses; Children under 6 months of age: ask a doctor.

Inactive Ingredients

Mica

Lauroyl lysine

Boron nitride

Silica

Triethoxycaprylylsilane

Ethyl ferulate

Oryza sativa (rice) bran extract

Iron oxides

Bisabolol

Squalane

Simmondsia chinensis (jojoba) seed oil

Glyceryl caprylate

Glycerin

Caprylhydroxamic acid

Other Information

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

label

INGREDIENTS AND APPEARANCE

BOB KIDS SPF 30 ZINC ONLY 
zinc oxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58274-021
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	22.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LEVOMENOL (UNII: 24WE03BX2T)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
ETHYL FERULATE (UNII: 5B8915UELW)
JOJOBA OIL (UNII: 724GKU717M)
RICE BRAN (UNII: R60QEP13IC)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
GLYCERIN (UNII: PDC6A3C0OX)
BORON NITRIDE (UNII: 2U4T60A6YD)
SQUALANE (UNII: GW89575KF9)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
MICA (UNII: V8A1AW0880)
LAUROYL LYSINE (UNII: 113171Q70B)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
FERRIC OXIDE RED (UNII: 1K09F3G675)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58274-021-01	3 g in 1 TUBE; Type 0: Not a Combination Product	06/12/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	06/12/2024

Labeler - SPF Ventures, LLC (055483891)

Establishment
Name	Address	ID/FEI	Business Operations
Innovation Labs, Inc		117109069	manufacture(58274-021)