ECLIPSE SPF 50 ALL SHADES- titanium dioxide, zinc oxide lotion 
SCIENCE OF SKINCARE LLC

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Eclipse SPF 50 Non Tinted

Active Ingredients

TITANIUM DIOXIDE – 5.20%

Zinc Oxide – 1.10%

PURPOSE

SUNSCREEN

USES

• Helps hydrate and 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

DIRECTIONS

• 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 of 15 or higher and other sun protection measures including:
o limit time in the sun, especially from 10 a.m.-2 p.m.
o wear long-sleeve shirts, pants, hats, and sunglasses
• Children under 6 months: Ask a doctor

Other Information

Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risk of skin cancer, and other harmful effects of the sun.

Questions or Comments?

Call Customer Care at (888) 804-4447

Inactive Ingredients

1,2-Hexanediol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Alumina, Butylene Glycol, C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Caprylyl Glycol, Cetearyl Alcohol, Cetearyl Glucoside, Disodium EDTA, Dimethicone, Glyceryl Stearate, Methicone, Octyldodecyl Neopentanoate, PEG-100 Stearate, Polyhydroxystearic Acid, Sorbitan Laurate, Styrene/Acrylates Copolymer, Tocopherol, Tocopheryl Acetate, Triethoxycaprylylsilane, VP/Eicosene Copolymer, Water/Aqua/Eau, Xanthan Gum +/- Iron Oxides.

Package Label - Principal Display Panel

300g Box NDC 69219-102-5310g Bag NDC 69219-102-21100g Label NDC 69219-102-01300g Label NDC 69219-102-03100g Box NDC 69219-102-1110g Label NDC 69219-102-02

ECLIPSE SPF 50  ALL SHADES
titanium dioxide, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69219-102
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE5.2 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION1.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
ALUMINUM (UNII: CPD4NFA903)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
PEG-100 STEARATE (UNII: YD01N1999R)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)  
STYRENE (UNII: 44LJ2U959V)  
TOCOPHEROL (UNII: R0ZB2556P8)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)  
WATER (UNII: 059QF0KO0R)  
XANTHAN GUM (UNII: TTV12P4NEE)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69219-102-511 in 1 BOX10/01/2014
1NDC:69219-102-1390 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2NDC:69219-102-111 in 1 BOX10/01/2014
2NDC:69219-102-01100 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3NDC:69219-102-211 in 1 BAG10/01/2014
3NDC:69219-102-0210 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4NDC:69219-102-03300 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2014
5NDC:69219-102-01100 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2014
6NDC:69219-102-0210 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2014
7NDC:69219-102-531 in 1 BOX08/01/2023
7300 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02010/01/2014
Labeler - SCIENCE OF SKINCARE LLC (006251958)

Revised: 12/2023
Document Id: 0c7e7997-ab76-2b88-e063-6294a90a4fff
Set id: 49df51e6-be9a-41be-b3e1-bfc062aaceaa
Version: 7
Effective Time: 20231214
 
SCIENCE OF SKINCARE LLC