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NDC 59779-0681-22 CVS Clear Face SPF 30 3 oz 2; 13; 5; 2; 4 g/100g; g/100g; g/100g; g/100g; g/100g Details

CVS Clear Face SPF 30 3 oz 2; 13; 5; 2; 4 g/100g; g/100g; g/100g; g/100g; g/100g

CVS Clear Face SPF 30 3 oz is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by CVS Pharmacy. The primary component is AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE.

Product Information

NDC	59779-0681
Product ID	59779-681_60379158-fb34-4515-8ce0-66d1c7b549eb
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	CVS Clear Face SPF 30 3 oz
Proprietary Name Suffix	n/a
Non-Proprietary Name	Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Product Type	HUMAN OTC DRUG
Dosage Form	LOTION
Route	TOPICAL
Active Ingredient Strength	2; 13; 5; 2; 4
Active Ingredient Units	g/100g; g/100g; g/100g; g/100g; g/100g
Substance Name	AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Labeler Name	CVS Pharmacy
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part352
Listing Certified Through	2024-12-31

Package

Package Images

NDC 59779-0681-22 (59779068122)

Pricing Information	N/A
NDC Package Code	59779-681-22
Billing NDC	59779068122
Package	88 g in 1 BOTTLE (59779-681-22)
Marketing Start Date	2016-06-02
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL b3b65560-4fa1-4bdb-8178-5d87ee2fd653 Details

Active Ingredients

Avobenzone 2.0%, Homosalate 13.0%, Octisalate 5.0%, Octocrylene 2.0%, Oxybenzone 4.0%

Purpose

Sunscreen

Uses

helps prevent sunburn
if used as directed with other sun protection measures (see Directions), decreases risk of skin cancer and early skin aging caused by the sun

Warnings

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

May stain some fabrics

Directions

apply liberally 15 minutes before sun exposure
reapply:
after 80 minutes of swimming or sweating
immediately after towel drying
at least every 2 hours
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 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

Inactive Ingredients

Water, Sorbitol, Triethanolamine, Aluminum Starch Octenylsuccinate, Benzyl Alcohol, Palmitic Acid, Sorbitan Isostearate, Stearic Acid, VP/Eicosene Copolymer, Dimethicone, Polyglyceryl-3 Distearate, Carbomer, Tocopherol, Disodium EDTA, Methylparaben, Propylparaben.

Other Information

protect this product from excessive heat and direct sun

Principle Display Panel

NDC 59779-681-22

CVS HEALTH

BREAKOUT FREE FACE LOTION

BROAD SPECTRUM SPF 30 SUNSCREEN

UVA/UVB protection

Lightweight and oil free

Won't clog pores, hypoallergenic

No added fragrance

Water resistant

(80 minutes)

Dermatologist tested

3.0 FL OZ (88 mL)

INGREDIENTS AND APPEARANCE

CVS CLEAR FACE SPF 30 3 OZ

avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:59779-681
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2 g in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	13 g in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2 g in 100 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	4 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
TROLAMINE (UNII: 9O3K93S3TK)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
BENZYL ALCOHOL (UNII: LKG8494WBH)
PALMITIC ACID (UNII: 2V16EO95H1)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
STEARIC ACID (UNII: 4ELV7Z65AP)
DIMETHICONE (UNII: 92RU3N3Y1O)
POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
TOCOPHEROL (UNII: R0ZB2556P8)
EDETATE DISODIUM (UNII: 7FLD91C86K)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:59779-681-22	88 g in 1 BOTTLE; Type 0: Not a Combination Product	06/02/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	06/02/2016

Labeler - CVS Pharmacy (062312574)

Revised: 6/2016

Document Id: 60379158-fb34-4515-8ce0-66d1c7b549eb

Set id: b3b65560-4fa1-4bdb-8178-5d87ee2fd653

Version: 1

Effective Time: 20160602