OTC Medication Information: Eucerin Q10 Anti-Wrinkle Sensitive Skin

EUCERIN Q10 ANTI-WRINKLE SENSITIVE SKIN- octinoxate, octisalate and oxybenzone lotion
Beiersdorf 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.

Active ingredients
Octinoxate 7.5%
Octisalate 3.0%
Oxybenzone 3.0%

Purpose
Sunscreen

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.

Stop use and ask a doctor if irritation occurs.

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

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

Uses • helps prevent sunburn

Directions
For sunscreen use: • apply liberally 15 minutes before sun exposure
• use a water resistant sunscreen if swimming or sweating
• reapply at least every 2 hours
• Children under 6 months of age: Ask a doctor

Inactive ingredients

Water, Glycerin, Cyclomethicone, Cetyl Alcohol, Methylpropanediol,

Alcohol Denat., Cetearyl Isononanoate, Glyceryl Stearate SE, Palmitic

Acid, Stearic Acid, Ubiquinone, Tocopheryl Acetate, Panthenol,

Caprylic/Capric Triglyceride, Octyldodecanol, Carbomer, Sodium

Hydroxide, Trisodium EDTA, Phenoxyethanol, Ethylhexylglycerin,

Piroctone Olamine.

Questions

800 227 4703

Eucerin

Q10 Anti-Wrinkle Face Lotion

SPF 15 Sunscreen

Coenzyme Q10 enriched formula

firms and moisturizes

for softer, smoother-looking skin

Non-Comedogenic Fragrance Free

Dermatological skincare

eucq10lotioncarton
(click image for full-size original)
EUCERIN Q10 ANTI-WRINKLE SENSITIVE SKIN
octinoxate, octisalate, oxybenzone lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:10356-340
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OCTINOXATE (OCTINOXATE) OCTINOXATE 7.5 g in 100 mL
OCTISALATE (OCTISALATE) OCTISALATE 3 g in 100 mL
OXYBENZONE (OXYBENZONE) OXYBENZONE 3 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
GLYCERIN
STEARIC ACID
CETYL ALCOHOL
CETEARYL ISONONANOATE
GLYCERYL MONOSTEARATE
ALCOHOL
MEDIUM-CHAIN TRIGLYCERIDES
OCTYLDODECANOL
UBIDECARENONE
.ALPHA.-TOCOPHEROL ACETATE, D-
PANTHENOL
EDETIC ACID
SODIUM HYDROXIDE
PHENOXYETHANOL
CYCLOMETHICONE
PALMITIC ACID
ETHYLHEXYLGLYCERIN
PIROCTONE OLAMINE
METHYLPROPANEDIOL
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL OR ALLYL SUCROSE CROSSLINKED)
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:10356-340-11 118 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part352 01/02/2001 06/30/2023
Labeler — Beiersdorf Inc (001177906)

Revised: 12/2022 Beiersdorf Inc

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2023. All Rights Reserved.