Daily Moisturizing Cream SPF 15

Daily Moisturizing SPF 15 by

Drug Labeling and Warnings

Daily Moisturizing SPF 15 by is a Otc medication manufactured, distributed, or labeled by Vivier Pharma Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DAILY MOISTURIZING SPF 15- octinoxate, octisalate, benzophenone cream 
Vivier Pharma 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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Daily Moisturizing Cream SPF 15

DRUG FACTS

ACTIVE INGREDIENTS

• 7.5%  Octinoxate
• 3.0%  Octyl Salicylate
• 3.0%  Benzophenone

PURPOSE

Sunscreen

USES

• Moisturizing cream with sunscreen.
• Helps prevent sunburn and provides a sun protection factor of 15.

WARNINGS

For external use only

When using this product

• Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Do not use

on damaged or broken skin.

Stop use and ask a doctor if

• Rash or irritation develops and lasts.

Keep out of reach of children

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

DIRECTIONS

• Apply to clean, dry skin, liberally and evenly 15 minutes before sun exposure.
• Reapply at least every 2 hours or as needed after towel drying, perspiring heavily or washing.
• For use on children less than 6 months of age, consult a healthcare practitioner.
• Use a water resistant sunscreen if swimming or sweating.

INACTIVE INGREDIENTS

WATER/EAU, SQUALANE, DIVINYLDIMETHICONE/DIMETHICONE COPOLYMER, C12-13 PARETH-23, C12-13 PARETH-3, XANTHAN GUM, CAPRYLYL GLYCOL, PHENOXYETHANOL, GLUCOSE, CARRAGEENANS (CHONDRUS CRISPUS), ETHYLHEXYLGLYCERIN, STEARYL ALCOHOL, TRIBEHENIN, POTASSIUM CETYL PHOSPHATE, HYDROGENATED PALM GLYCERIDES, GLYCERIN, GLYCERYL POLYACRYLATE, POLYACRYLAMIDE, C13-14 ISOPARAFFIN, LAURETH-7, CETYL PALMITATE, METHYLPARABEN, BUTYLPARABEN, ETHYLPARABEN, PROPYLPARABEN, TOCOPHERYL ACETATE, PROPYLENE GLYCOL, DIAZOLIDINYL UREA, IODOPROPYNYL BUTYLCARBAMATE, ALLANTOIN, SODIUM HYALURONATE, HYDROLYZED GLYCOSAMINOGLYCANS, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, SODIUM ASCORBYL PHOSPHATE

Questions?

450 455 9779     1 877 484 8437

Package Labeling:

DAILY MOISTURIZING SPF 15 
octinoxate, octisalate, benzophenone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67226-2015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	30 mg  in 1 mL
BENZOPHENONE (UNII: 701M4TTV9O) (BENZOPHENONE - UNII:701M4TTV9O)	BENZOPHENONE	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SQUALANE (UNII: GW89575KF9)
C12-13 PARETH-23 (UNII: J1WW1510L4)
C12-13 PARETH-3 (UNII: DMC6N3419L)
XANTHAN GUM (UNII: TTV12P4NEE)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
CHONDRUS CRISPUS (UNII: OQS23HUA1X)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
GLYCERIN (UNII: PDC6A3C0OX)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
LAURETH-7 (UNII: Z95S6G8201)
CETYL PALMITATE (UNII: 5ZA2S6B08X)
METHYLPARABEN (UNII: A2I8C7HI9T)
BUTYLPARABEN (UNII: 3QPI1U3FV8)
ETHYLPARABEN (UNII: 14255EXE39)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
ALLANTOIN (UNII: 344S277G0Z)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ROSEMARY (UNII: IJ67X351P9)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67226-2015-5	48 mL in 1 JAR; Type 0: Not a Combination Product	11/11/2017	11/30/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	11/11/2017	11/30/2019

Labeler - Vivier Pharma Inc (250996550)

Revised: 1/2020

Document Id: 9d7229c6-406a-fe46-e053-2995a90a5dd1

34390-5

Set id: 803ba287-a2dd-4249-959d-00e3fcc0e165

Version: 5

Effective Time: 20200131