DEFENSE BROAD SPECTRUM SPF 25 SUNSCREEN- octinoxate and zinc oxide lotion

Defense Broad Spectrum SPF 25 Sunscreen by

Drug Labeling and Warnings

Defense Broad Spectrum SPF 25 Sunscreen by is a Otc medication manufactured, distributed, or labeled by Emerald Aesthetics LLC, COSMETIC SOLUTIONS, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

DRUG FACTS:

ACTIVE INGREDIENTS

Octinoxate 7.0%, Zinc Oxide 6.0%.

PURPOSE

Sunscreen

USES

Helps prevent sunburn.

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.

DIRECTIONS

Apply to all skin exposed to the sun.

• Apply liberally and evenly 15 minutes before sun exposure.
• Reapply at least every 2 hours.
• Use a water-resistant sunscreen if swimming or sweating.
• For children under 6 months of age: Ask a doctor.

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 value 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-sleeved shirts, pants, hats, and sunglasses.

INACTIVE INGREDIENTS

Water, Isocetyl Stearate, Cetyl Dimethicone, Styrene/Acrylates Copolymer, Sorbitol, Ethyl Macadamiate, Cetearyl Alcohol, Dimethicone, Acrylates/Dimethicone Copolymer, Phenoxyethanol, Glyceryl Stearate, Glycerin, Hydroxyethyl Acrylate/ Sodium Acryloyldimethyl Taurate Copolymer, PEG-100 Stearate, Ceteareth-20, Ethylhexyl Salicylate, VP/Eicosene Copolymer, Xanthan Gum, Polymethyl Methacrylate, Caprylyl Glycol, Cocos Nucifera Oil, Ethylhexylglycerin, Vaccinium Vitis-Idaea Fruit Extract, Quercus Suber Bark Extract, Triethoxycaprylylsilane, Camellia Sinensis Leaf Extract, Disodium EDTA, Tocopheryl Acetate, Oak Root Extract, Centella Asiatica Extract, Polygonum Aviculare Extract, Citric Acid, Gluconolactone, Isomalt, Calcium Gluconate, Lecithin, Vitis Vinifera Fruit Cell Extract, Sodium Benzoate, Lepidium Sativum Sprout Extract.

OTHER INFORMATION

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

PRINCIPAL DISPLAY PANEL

Defense Broad Spectrum SPF 25 Sunscreen

INGREDIENTS AND APPEARANCE

DEFENSE BROAD SPECTRUM SPF 25 SUNSCREEN 
octinoxate and zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82670-2650
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7 g  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOCETYL STEARATE (UNII: 3RJ7186O9W)
SORBITOL (UNII: 506T60A25R)
ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIMETHICONE (UNII: 92RU3N3Y1O)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
PEG-100 STEARATE (UNII: YD01N1999R)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
OCTISALATE (UNII: 4X49Y0596W)
XANTHAN GUM (UNII: TTV12P4NEE)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LINGONBERRY (UNII: 0UNK9RZQ7X)
QUERCUS SUBER BARK (UNII: 8R5219271Q)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
ISOMALT (UNII: S870P55O2W)
CALCIUM GLUCONATE (UNII: SQE6VB453K)
SODIUM BENZOATE (UNII: OJ245FE5EU)
GARDEN CRESS SPROUT (UNII: PWQ18YNR62)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82670-2650-2	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	03/01/2023

Labeler - Emerald Aesthetics LLC (087054382)

Establishment
Name	Address	ID/FEI	Business Operations
COSMETIC SOLUTIONS, LLC		807907928	manufacture(82670-2650)