DAY L- avobenzone octisalate octinoxate lotion 
Kamins Dermatologics Inc.

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CONSUMER LABELING

Active ingredients:

AVOBENZONE 2.5 %

OCTINOXATE 7.5 %

OCTISALATE 4.0 %

Purpose: Sunscreen

Keep out of the reach of children.

A LIGHT, SILKY LOTION THAT DIFFUSES A BLEND OF MOISTURIZERS, ANTI-OXYDANT VOTMINS INTO THE SKIN TO ENHANCE DAY LONG COMFORT AND HYDRATION. THE SKIN'S OUTER LAYERS ARE COVERED WITH A PROTECTIVE SHIELD, PRODUCING A HEALTHY, LUMINESCENT GLOW. 

Uses

■ Helps prevent sunburn.

■ Higher SPF gives more sunburn protection.

■ Provides moderate protection against sunburn.

Warnings

For external use only.

When using this product, keep out of eyes. If contact occurs, rinse abundantly with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

If swallowed, seek medical assistance or contact a Poison Control Center immediately.





Directions:

Apply liberally and evenly each morning to cleansed face and neck, before sun exposure and as needed.

Children under 6 months of age: ask a doctor.

Inactive ingredients:

aqua/water/eau, acer saccharum (maple isolate), butylene glycol, hydrolyzed collagen, hydrolyzed elastin, octocrylene, cetyl alcohol, glyceryl stearate SE, ceteareth-12, cyclotetrasiloxane, cyclopentasiloxane, PEG/PPG-18/18 dimethicone, coco- caprylate/caprate, polysorbate-80, carbomer, tocopheryl acetate, retinyl palmitate, sodium hydroxide, phenoxyethanol, caprylyl glycol, sorbic acid, parfum/fragrance

B. KAMINS

DAY LOTION SPF15

50mL / 1.7 fl.oz

DIN 02248016


Day Lotion front panel image

DAY L 
avobenzone octisalate octinoxate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63550-122
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE25 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE40 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
SORBIC ACID (UNII: X045WJ989B)  
WATER (UNII: 059QF0KO0R)  
ACER SACCHARUM SAP (UNII: 75UOH57984)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
HYDROLYZED BOVINE ELASTIN (BASE; 1000 MW) (UNII: ZR28QKN0WT)  
OCTOCRYLENE (UNII: 5A68WGF6WM)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
CETEARETH-12 (UNII: 7V4MR24V5P)  
CYCLOMETHICONE 4 (UNII: CZ227117JE)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
COCO-CAPRYLATE (UNII: 4828G836N6)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63550-122-0350 mL in 1 BOX; Type 0: Not a Combination Product03/01/200412/31/2023
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02003/01/200412/31/2023
Labeler - Kamins Dermatologics Inc. (254050784)
Registrant - Kamins Dermatologics Inc. (254050784)
Establishment
NameAddressID/FEIBusiness Operations
Odan Laboratories Ltd208585604manufacture(63550-122)

Revised: 6/2024
 
Kamins Dermatologics Inc.