VERTRA ELEMENT RESISTANCE DAILY DRIVER SPF30- homosalate, octisalate, avobenzone, octocrylene lotion
Northwest Cosmetic Laboratories

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.

----------

Vertra Daily Driver Sunscreen Moisturizer and Anti-Aging SPF30

Daily Driver

VERTRA ELEMENT RESISTANCE DAILY DRIVER SPF30
homosalate, octisalate, avobenzone, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62282-371
Route of Administration	topical

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	5.0 g in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5.0 g in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3.0 g in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2.7 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
AMMONIUM ACRYLOYLDIMETHYLTAURATE (UNII: KBC00G95HI)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CHLORPHENESIN (UNII: I670DAL4SZ)
CITRUS SINENSIS FRUIT OIL (UNII: WV48LBL15Q)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)
DIMETHICONE (UNII: 92RU3N3Y1O)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ABELMOSCHUS ESCULENTUS WHOLE (UNII: 505GKC6541)
ISODODECANE (UNII: A8289P68Y2)
PEG-100 STEARATE (UNII: YD01N1999R)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYURETHANE-34 (40 MPA, TENSILE STRENGTH OF FILM AT BREAK) (UNII: 77KA3O6NNF)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
STARCH, TAPIOCA (UNII: 24SC3U704I)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
water (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:62282-371-02	1 in 1 CARTON	02/01/2019
1	NDC:62282-371-01	50 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	02/01/2019	06/03/2022

Labeler - Northwest Cosmetic Laboratories (929572014)

Revised: 6/2022

Document Id: 859ce9f5-b10e-4340-88be-5980d52d61f5

Set id: 333e4de0-83b7-4b48-8e31-b462b6dce4f8

Version: 8

Effective Time: 20220606

Northwest Cosmetic Laboratories