LIGHT AND DELICATE SUNSCREEN SPF15- avobenzone, benzophenone-3, homosalate, octinoxate, octisalate, octocrylene lotion

LIGHT AND DELICATE SUNSCREEN SPF15 by

Drug Labeling and Warnings

LIGHT AND DELICATE SUNSCREEN SPF15 by is a Otc medication manufactured, distributed, or labeled by Genuine Virgin Aloe Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENT

• AVOBENZONE 3%
• BENZOPHENONE-3  5%
• HOMOSALATE  5%
• OCTINOXATE  7.49%
• OCTISALATE  5%
• OCTOCRYLENE  2.7%

DOSAGE & ADMINISTRATION

DIRECTIONS

•  FOR DAILY USE, ALLOW PRODUCT TO ABSORB COMPLETELY BEFORE APPLYING MAKE-UP
•  APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE
•  REAPPLY AS NEEDED OR AFTER TOWEL DRYING, SWIMMING, OR PERSPIRING
•  SUN PROTECTION MEASURES
•  SPEDNING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY
•  AGEING. TO DECREASE THIS RISK, REGULARLY USE A SUNSCREEN WITH A BROAD
•  SPECTRUM SPF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUDING
•  LIMITING TIME IN THE SUN, ESPECIALLY FROM 10 AM TO 2 PM.
•  WEAR LONG SLEEVE SHIRTS, PANTS, HATS AND SUNGLASSES
•  FOR USE ON CHILDREN 6 MONTHS AND OLDER/ CHILDREN UNDER 6 MONTHS ASK A DOCTOR

PURPOSE

PURPOSE:

• SUNSCREEN

INDICATIONS & USAGE

Uses:

• DAILY MOISTURIZER
• 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.

WARNINGS

WARNINGS

FOR EXTERNAL USE ONLY

WHEN USING

WHEN USING THIS PRODUCT

• KEEP OUT OF THE EYES.
• RINSE WITH WATER TO REMOVE

STOP USE

STOP USE AND ASK A DOCTOR IF

• IF RASH OR IRRITATION DEVELOPS AND LASTS

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

• IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

INACTIVE INGREDIENT

Inactive ingredients: ALARIA ESCULENTA EXTRACT, BEHENYL ALCOHOL, BETAINE, C12-15 ALKYL BENZOATE,

CAPRYLIC/CAPRIC TRIGLYCERIDE, CETYL ALCOHOL, DIISOPROPYL SEBACATE, DISODIUM EDTA, GLUCONO LACTONE,

GLYCERIN, GLYCERYL STEARATE, LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE, LONICERA CAPRIFOLIUM (HONEYSUCKLE)

FLOWER EXTRACT, LONICERA JAPONMICA (HONEYSUCKLE) FLOWER EXTRACT, PANTHENOL, POPULUS TREMULOIDES BARK EXTRACT,

POTASSIUM CETYL PHOSPHATE, POTASSIUM SORBATE, SODIUM HYALURONATE, TOCOPEROL, WATER(AQUA), XANTHAN GUM

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIGHT AND DELICATE SUNSCREEN SPF15 
avobenzone, benzophenone-3, homosalate, octinoxate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10738-014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	5 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	5 g  in 100 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.49 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2.70 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALARIA ESCULENTA (UNII: EJ9JK8J58D)
DOCOSANOL (UNII: 9G1OE216XY)
BETAINE (UNII: 3SCV180C9W)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
PANTHENOL (UNII: WV9CM0O67Z)
POPULUS TREMULOIDES BARK (UNII: 5543O0CEID)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10738-014-17	48 g in 1 TUBE; Type 0: Not a Combination Product	08/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	08/01/2016

Labeler - Genuine Virgin Aloe Corporation (743159706)

Registrant - Genuine Virgin Aloe Corporation (743159706)