CYBERDERM EVERY MORNING SUN WHIP- zinc oxide, octinoxate lotion 
Cyberderm Laboratories 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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Cyberderm Every Morning Sun Whip™ Sunscreen SPF 25

Drug Facts

Active ingredients

Octinoxate (encapsulated) 7.5%

Zinc oxide* 15%

Purpose

Sunscreen

Uses

Helps prevent sunburn

Warnings

Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

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

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:

Other information

Inactive ingredients water/eau, caprylic/capric triglyceride*, glyceryl isostearate*, polyhydroxystearic acid*, glyceryl stearate*, PEG-75 stearate, ceteth-20, steareth-20, glycerin*, cetyl dimethicone, methylcellulose, trisodium ethylenediame disuccinate, xanthan gum, sclerotium gum, caprylhydroxamic acid, caprylyl glycol, silica, PVP, chlorphenesin, cetyl alcohol, sodium citrate, phenoxyethanol, disodium EDTA, BHT

Questions or comments?

781-481-2628 Monday - Friday 9 am - 5 pm

*Denotes ingredients that are Ecocert® certified organic.

Distributed by:

CyberDERM Laboratories Incorporated

650-1600 Carling Avenue

Ottawa, ON K1Z 1G3 Canada

Made in Canada

cyberderm

made with love by the sunscreen company™

Every Morning Sun Whip™ SPF 25

Transparent sunscreen lotion

made with 15% zinc oxide and 7.5% encapsulated octinoxate

SPF 25 Sunscreen

helps prevent sunburn

50 mL (1.7 fl oz)

EM - Box FDA 2018-4-5

CYBERDERM  EVERY MORNING SUN WHIP
zinc oxide, octinoxate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71644-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION15 g  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM (UNII: 7FLD91C86K)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
METHYLCELLULOSE (15 MPA.S) (UNII: NPU9M2E6L8)  
WATER (UNII: 059QF0KO0R)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
GLYCERIN (UNII: PDC6A3C0OX)  
XANTHAN GUM (UNII: TTV12P4NEE)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-75 STEARATE (UNII: OT38R0N74H)  
CETETH-20 (UNII: I835H2IHHX)  
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
STEARETH-20 (UNII: L0Q8IK9E08)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
BETASIZOFIRAN (UNII: 2X51AD1X3T)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)  
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71644-004-501 in 1 CARTON03/30/2018
150 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:71644-004-801 in 1 CARTON03/30/2018
280 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35203/30/2018
Labeler - Cyberderm Laboratories Inc. (242524267)

Revised: 1/2023
Document Id: f1ffd8e8-c558-43d7-e053-2a95a90a316e
Set id: 69342d1d-027a-410b-e053-2a91aa0a3512
Version: 2
Effective Time: 20230111
 
Cyberderm Laboratories Inc.