POWDER- zinc oxide, titanium dioxide powder

powder by

Drug Labeling and Warnings

powder by is a Otc medication manufactured, distributed, or labeled by Oxygen development, Oxygen Development. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Titanium Dioxide 8.6

zinc Oxide 10.0

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 again caused by the sun.

Warnings

For external use only

Stop Use

Stop use and ask doctor if rash occurs

Do not use

Do not use on damaged or broken skin

When using

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

Keep out of the reach of children

If swallowed, get medical help or contact a Poison Control center rigth away

Directions

Apply liberally 15 minutes before sun exposure. Use a water resistant sunscreen if swimming or sweating. reapply at lease every 2 hours. Children under 6 months: ask a doctor. optional: apply toall skin exposed to the sun. Sun Protection measures. spending time in the sin increases your risk ofg skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m-2p.m. Wear long-sleeved shirts, pants, hats and sunglasses.

Other information

Protect the product in this container from excessive heat and direct sunlight. You may report a serious adverse reaction to: tarte c/o report Reaction, LLC,P.O.Box 22,Plainsboro, New Jersey 08536-0222.

Primary package

Secondary Package

INGREDIENTS AND APPEARANCE

POWDER 
zinc oxide, titanium dioxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61354-052
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	8.6 mg  in 100 mg
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	10 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
JOJOBA OIL (UNII: 724GKU717M)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61354-052-01	1 in 1 CARTON	02/23/2021
1		8 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	02/22/2021

Labeler - Oxygen development (137098492)

Establishment
Name	Address	ID/FEI	Business Operations
Oxygen Development		137098492	manufacture(61354-052)