DR. MERCOLA Sunscreen Broad Spectrum SPF-30

Active Ingredient

Zinc Oxide (20%)

Purpose

Sunscreen

Uses

Helps prevent sunburn
If used as directed with other sun protection measures (see Directions), sunscreen decreases the risk of skin cancer and early skin aging caused by the sun.

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 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.
Children under 6 months of age: Ask a doctor.
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: Sun Protection Measures:
- Limit time in the sun, especially from 10 a.m. - 2 p.m.
- Wear long-sleeve shirts, pants, hats, and sunglasses
Re-apply:
- After 40 minutes of swimming or sweating
- Immediately after towel drying
- At least every 2 hours

Other Information

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

Inactive Ingredients

Aqua, Aloe Barbadensis Leaf Juice, Helanthus Annuus (Sunflower) Seed Oil, Lecithin, Cetearyl Alcohol, Cetearyl Glucoside, Cetearyl Olivate, Sorbitan Olivate, Glycerin, Simmonds Chinensia (Jojoba) Seed Oil, Butyrospermum ParkII (Shea) Butter, Camellia Sinensis Leaf Extract, Cocos Nucifera (Coconut) Oil, Glucurolactone, Potassium Sorbate, Xanthan Gum, Punica Granalum Fruit Extract, Tocopherol, Rubus Idaeus (Raspberry) Seed Oil, Astaxanthain Eucalyptus Globulus Leaf Oil.

DR. MERCOLA Sunscreen Broad Spectrum SPF-30

SPF 30

DR. MERCOLA SUNSCREEN BROAD SPECTRUM SPF-30
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:65121-883
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	200 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SUNFLOWER OIL (UNII: 3W1JG795YI)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
SORBITAN OLIVATE (UNII: MDL271E3GR)
GLYCERIN (UNII: PDC6A3C0OX)
JOJOBA OIL (UNII: 724GKU717M)
SHEA BUTTER (UNII: K49155WL9Y)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
COCONUT OIL (UNII: Q9L0O73W7L)
GLUCUROLACTONE (UNII: XE4Y3016M9)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
XANTHAN GUM (UNII: TTV12P4NEE)
POMEGRANATE (UNII: 56687D1Z4D)
TOCOPHEROL (UNII: R0ZB2556P8)
RASPBERRY SEED OIL (UNII: 9S8867952A)
ASTAXANTHIN (UNII: 8XPW32PR7I)
EUCALYPTUS OIL (UNII: 2R04ONI662)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:65121-883-30	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/09/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	04/28/2014

Labeler - Pure Source, LLC (080354456)

Name	Address	ID/FEI	Business Operations
Establishment
Pure Source, LLC		080354456	manufacture(65121-883)