Daily Facial Moisturizer SPF 25: Package Insert and Label Information

DAILY FACIAL MOISTURIZER SPF 25- homosalate, avobenzone, octinoxate and octocrylene cream
Person and Covey

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.

Uses

-Moisturizes and helps to relieve irritated and sensitive skin

-Higher SPF gives more sunburn protection

-Water resistant

Keep Out of the Reach of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Warnings

For external use only

.Stop Use

Stop Use and ask a Doctor if a rash rash or irritation develops and lasts

Questions

Questions? Please call 1 (800) 423-2341

Inactive Ingredients

Purified Water, Propylene Glycol Dioctanoate, Petrolatum, Glycerin, Glyceryl Stearate, PEG-100 Stearate, DEA-Cetyl Phosphate, Stearic Acid, Hyaluronic Acid, Benzyl Alcohol, Dimethicone, Cyclomethicone, PVP/Eicosene Copolymer, Silica, Sodium Carbomer 941, Allantoin, Disodium EDTA, Magnesium Aluminum Silicate

Other Information

-High sun protection product

-Sun Alert: limiting sun exposure, wearing sun protective clothing and using sunscreens may reduce the risk of skin aging, skin cancer and other harmful effects of the sun.

-Avoid exposure to extreme heat or cold.

Active Ingredients

Octinoxate……7.5% Sunscreen

Homosalate….6.0% Sunscreen

Avobenzone…3.0% Sunscreen

Octocrylene….1.5% Sunscreen

Directions

-Apply DML Daily Facial Moisturizer liberally and evenly 15-20 minutes before sun exposure and message in gently, allowing it to dry. Reapply as needed or as directed by your Dermatologist.

-DML Daily Facial is an excellant make-up base.

Purpose

Sunscreen

Package Label Principal Display Panel

DML Facial Moisturier
(click image for full-size original)

DAILY FACIAL MOISTURIZER SPF 25
sunscreen cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0096-0721
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HOMOSALATE (HOMOSALATE) HOMOSALATE 0.06 g in 1 g
AVOBENZONE (AVOBENZONE) AVOBENZONE 0.03 g in 1 g
OCTINOXATE (OCTINOXATE) OCTINOXATE 0.075 g in 1 g
OCTOCRYLENE (OCTOCRYLENE) OCTOCRYLENE 0.015 g in 1 g
Inactive Ingredients
Ingredient Name Strength
DIMETHICONE 1000
SILICON DIOXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0096-0721-07 7 g in 1 BOTTLE None
2 NDC:0096-0721-45 45 g in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part352 08/01/1991
Labeler — Person and Covey (008482473)
Establishment
Name Address ID/FEI Operations
Person and Covey 008482473 manufacture (0096-0721)

Revised: 11/2018 Person and Covey

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2021. All Rights Reserved.