Drug Facts

Active Ingredients

Octinoxate 5.0%
Zinc Oxide 5.1%

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

Directions

apply generously 15 minutes before sun exposure
reapply at least every 2 hours
use a water resistant sunscreen if swimming or sweating
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 10am - 2pm
- wear long-sleeved shirts, pants, hats, and sunglasses
children under 6 months of age: ask a doctor

Inactive Ingredients

Cyclopentasiloxane, Ascorbic Acid, Ethylhexyl Hydroxystearate, Polysilicone-11, Caprylic/Capric Triglyceride, Cetyl PEG/PPG-10/1 Dimethicone, Polyester-7, Tocopherol, Creatine, Epigallocatechin Gallate, Triethoxycaprylylsilane, Neopentyl Glycol Diheptanoate, Disteardimonium Hectorite, Polyhydroxystearic Acid, Propylene Carbonate, Dimethylmethoxy Chromanol, BHT

Other Information

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

Questions?

1.844.469.6379

PRINCIPAL DISPLAY PANEL - 30 ML Bottle Carton

reactive+

ANTI-OXIDANT SERUM +
BROAD-SPECTRUM SPF 45

NEOCUTIS®

Principal Display Panel - 30 ML Bottle Carton

REACTIVE PLUS ANTI-OXIDANT SERUM PLUS BROAD-SPECTRUM SPF 45
octinoxate and zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:46783-222
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	50 mg in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	51 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
ETHYLHEXYL HYDROXYSTEARATE (UNII: B7I80BVV5E)
POLYSILICONE-15 (UNII: F8DRP5BB29)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
POLYESTER-7 (UNII: 0841698D2F)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CREATINE (UNII: MU72812GK0)
EPIGALLOCATECHIN GALLATE (UNII: BQM438CTEL)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
DIMETHYLMETHOXY CHROMANOL (UNII: XBH432G01F)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:46783-222-30	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC:46783-222-04	4 mL in 1 TUBE; Type 0: Not a Combination Product	06/15/2019	04/04/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

Labeler - Merz North America, Inc (028147846)

Réactive+ Anti-Oxidant Serum plus Broad-spectrum SPF 45