ELTA MD- zinc oxide spray

Elta MD by

Drug Labeling and Warnings

Elta MD by is a Otc medication manufactured, distributed, or labeled by CP Skin Health Group, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 physician

if rash occurs

Inactive Ingredients

Caprylic/Capric Triglyceride, Helianthys Annuus (Sunflower) Seed Wax, Cerearyl Nonanoate, Theobroma Cacao Cocoa) Seed Butter, Butyloctyl Salicylate, Lauryl Laurate, Polyhydroxystearic Acid, Euphorbia Cerifera (Candelilla) Was, Capryloyl Glycerin/Sebacic Acid Copolymer, Mica, Behenyl Behenate, Butyrospermum Parkii (Shea) Butter, Oryzanol, Ethyl Ferulate, Isostearic Acid, Lecithin, Polyglyceryl-3 Plyricinoleate, Bisabolol, Tocopherol, Silica

Uses

helps prevent sunburn
if used as directed with other sun protection measures (see​Directions​), decreases the risk of UV damage and early skin aging caused by the sun

KEEP OUT OF REACH OF CHILDREN

If product is swallowed, get medical help or contact a Poison Control Center right away.

PURPOSE

Sunscreen

DOSAGE & ADMINISTRATION

Apply liberally 15 minutes before sun exposure
Reapply: after 80 minutes of swimming or sweating: immediately after towel drying: at lear every 2 hours
Sun Protection Measures

Spending time in the sun can increase your riske of skin cancer and early skin aging.
To decrease this risk regularly use a sunscreen with a broad spectrum SPF 15 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-sleeve shirts, pants, hats, and sunglasses
Children under 6 months:Ask a physician

Elta MD UV Active Spray

INGREDIENTS AND APPEARANCE

ELTA MD 
zinc oxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72043-4341
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	14 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72043-4341-1	1 in 1 CARTON	12/14/2023
1		170 g in 1 BOTTLE, SPRAY; 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	12/14/2023

Labeler - CP Skin Health Group, Inc. (611921669)