MICRO DAY REJUVENATING BROAD-SPECTRUM SUNSCREEN SPF 30- octinoxate and zinc oxide lotion 
Merz North America, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Micro Day Rejuvenating Cream Broad-spectrum Sunscreen SPF 30

Drug Facts

Active ingredients

Octinoxate 7.5%

Zinc Oxide 7.3%

Purpose

Sunscreen

Uses

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. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

See package insert for complete information.

For sunscreen use:

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 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

Water, Caprylic/Capric Triglyceride, Hydrogenated C6-14 Olefin Polymers, Hexyldecanol, Glycerin, Glyceryl Stearate, PEG-100 Stearate, Potassium Cetyl Phosphate, Hydrogenated Palm Glycerides, Microcrystalline Cellulose, Camelia Sinensis Extract, Silica, Tetrapeptide-21, Capryloyl Carnosine, Palmitoyl Tripeptide-1 Acetate, Sodium Ascorbyl Phosphate, Tocopheryl Acetate, Squalane, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyhydroxystearic Acid, Steareth-21, Melanin, Cetearyl Alcohol, Sodium Hyaluronate, Polysorbate 60, Triethoxycaprylsilane, Disodium EDTA, Xanthan Gum, Cellulose Gum, Styrene/Acrylates Copolymer, Phenoxyethanol, Methylparaben, Ethylparaben, Propylparaben.

Other information

Questions?

USA: 866.636.2884 • International: +800.1489.1489

Distributed in the USA by Merz North America, Inc.

PRINCIPAL DISPLAY PANEL - 50 ML Bottle Carton

micro day®

REVITALIZING
& TIGHTENING
DAY CREAM
SPF 30

NEOCUTIS®

PRINCIPAL DISPLAY PANEL - 50 ML Bottle Carton
MICRO DAY REJUVENATING BROAD-SPECTRUM SUNSCREEN SPF 30 
octinoxate and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46783-173
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE73 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
HEXYLDECANOL (UNII: 151Z7P1317)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ETHYLPARABEN (UNII: 14255EXE39)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
STEARETH-21 (UNII: 53J3F32P58)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
HYDROGENATED POLY(C6-14 OLEFIN; 2 CST) (UNII: P0TX083987)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46783-173-051 in 1 CARTON03/23/201502/28/2023
115 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:46783-173-101 in 1 CARTON03/23/201512/31/2022
230 mL in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:46783-173-201 in 1 CARTON03/23/201512/31/2022
3200 mL in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:46783-173-044 mL in 1 TUBE; Type 0: Not a Combination Product06/15/201910/31/2024
5NDC:46783-173-501 in 1 CARTON10/20/201912/31/2023
550 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35203/23/201510/31/2024
Labeler - Merz North America, Inc. (028147846)

Revised: 6/2023
Document Id: ec4a7869-c831-47e7-8c12-352a16a2424b
Set id: d4cc35c9-3f53-4bb0-98db-97a59c5b3d7d
Version: 8
Effective Time: 20230628
 
Merz North America, Inc.