DAILY DRIVER SUNSCREEN BROAD SPECTRUM SPF 30- homosalate, octisalate, avobenzone, octocrylene cream

Daily Driver Sunscreen Broad Spectrum SPF 30 by

Drug Labeling and Warnings

Daily Driver Sunscreen Broad Spectrum SPF 30 by is a Otc medication manufactured, distributed, or labeled by Eai-jr 286, Inc, Northwest Cosmetic Laboratories LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients Purpose

Homosalate 5% Sunscreen

Octisalate 5% Sunscreen

Avobenzone 3% Sunscreen

Octocrylene 2.7% Sunscreen

PURPOSE

Uses

• Helps prevent Sunburn
• If used as directed with other sun protection measures ( see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

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

INDICATIONS & USAGE

Stop use and ask a doctor if rash occurs

WARNINGS

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

DOSAGE & ADMINISTRATION

Directions

Apply liberally and generously 15 minutes before sun exposure and at least
every 2 hours.

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 value of 15 or higher and other sun
protection measures including: limit your 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 INGREDIENT

Inactive ingredients:

Water, Isododecane, Dimethicone, Glycerin, Tapioca starch, Pentylene Glycol, Cetearyl Alcohol, Polyurethane-34, Polysilicone-11, Isododecane, Coco-Caprylate/-Caprate, Glyceryl Stearate, PEG-100 Stearate, Phenoxyethanol, Hydrolyzed Hibiscus Esculentes Extract, Butylene Glycol, SOdium Polyacrylate, Dextrin, Citrus Sinensis (Blood Orange) Fruit Extract, Aloe Barbadensis Leaf Extract, Caprylyl Glycol, Ethylhexyl Stearate, Xanthan Gum, Ammonium Acryloyldeimethyltaurate/VP Copolymer, Fragrance, Chlorphenesin, Aloe Barbadensis Leaf Juice, Sodium Citrate, Tocopheryl Acetate, Trideceth-6, Leuconostoc/Radish root ferment Filtrate, Disodium EDTA, Decyl Glucoside, Caprylyl Glycol, Phenoxyethanol, Hexylene Glycol, Aminomethyl Propanol

PRINCIPAL DISPLAY PANEL

Daily Driver

Sun Resistance & anti-aging

Face and Body Lotion

Broad Spectrum SPF 30

Color: Untinted

INGREDIENTS AND APPEARANCE

DAILY DRIVER SUNSCREEN BROAD SPECTRUM SPF 30 
homosalate, octisalate, avobenzone, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71014-013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	5 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2.7 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
XANTHAN GUM (UNII: TTV12P4NEE)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)
CITRUS SINENSIS WHOLE (UNII: 37673443KL)
CHLORPHENESIN (UNII: I670DAL4SZ)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
STARCH, TAPIOCA (UNII: 24SC3U704I)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POLYURETHANE-34 (40 MPA, TENSILE STRENGTH OF FILM AT BREAK) (UNII: 77KA3O6NNF)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
ICODEXTRIN (UNII: 2NX48Z0A9G)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
PEG-100 STEARATE (UNII: YD01N1999R)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
ISODODECANE (UNII: A8289P68Y2)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71014-013-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	11/02/2018

Labeler - Eai-jr 286, Inc (827896718)

Establishment
Name	Address	ID/FEI	Business Operations
Northwest Cosmetic Laboratories LLC		929572014	manufacture(71014-013)