Cyberderm

Manufacturer
Cyberderm Laboratories Inc.
Effective date
2023-01-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:40:47

Label at a glance#

ProductCyberderm Every Morning Sun Whip
Active ingredientZINC OXIDE, OCTINOXATE
Label structure15 sections

Storage and handling

Other information Protect this product from excessive heat and direct sun May stain some fabrics

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Octinoxate (encapsulated) 7.5%

Zinc oxide* 15%

OTC - PURPOSE SECTION

Purpose

Sunscreen

INDICATIONS & USAGE SECTION

Uses

Helps prevent sunburn

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply liberally to face and body 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 10 a.m.-2 p.m.
  • Wear long-sleeved shirts, pants, hats and sunglasses
  • Children under 6 months of age: ask a doctor

STORAGE AND HANDLING SECTION

Other information

  • Protect this product from excessive heat and direct sun
  • May stain some fabrics

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

Questions or comments?

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

SPL UNCLASSIFIED SECTION

*Denotes ingredients that are Ecocert® certified organic.

Distributed by:

CyberDERM Laboratories Incorporated

650-1600 Carling Avenue

Ottawa, ON K1Z 1G3 Canada

Made in Canada

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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 2018-4-5EM - Box FDA 2018-4-5

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71644-00471644-004-50, 71644-004-80

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
28f5a61e-0f93-961c-e063-6294a90a0f4269342d1d-027a-410b-e053-2a91aa0a35122025-01-01WarningsExact identifier
spl set id: 69342d1d-027a-410b-e053-2a91aa0a3512

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.