Drug Facts

Active Ingredients:

Avobenzone (3.0%)

Octinoxate (7.5%)

Octisalate (5.0%)

Oxybenzone (4.0%)

Purpose:

Sunscreen

Uses

helps prevent sunburn
if used as directed with other sun protection measures (see Directions), helps decrease the 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 the eyes. Rinse with water to remove.

Stop use and ask a doctor if skin rash occurs.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply liberally 15 minutes before sun exposure
use a water resistant sunscreen if swimming or sweating
reapply at least every 2 hours
Children under 6 months of age: Ask a doctor
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 time in the sun, especially from 10 a.m. – 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses

Other information

protect the product in this container from excessive heat and direct sun

Inactive ingredients

Aqua (Water/Eau)

Isoeicosane

Potassium Cetyl Phosphate

Cetearyl Alcohol

Cetyl Dimethicone

Dimethicone

Ethyhexyl Methoxycrylene

Glycerin

Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer

Silica

Sorbitan Sesquioleate

Isohexadecane

Phenoxyethanol

Caprylyl Glycol

Ethylhexylglycerin

Polysorbate 60

Hexylene Glycol

Citric Acid

MAY CONTAIN (+/-):

Titanium Dioxide (CI 77891)

Iron Oxides (CI 77491, CI 77492, CI 77499)

Principal Display Panel - 50mL Carton Label

SUNSCREEN

broad
spectrum
spf 30

glo·therapeutics

Moisturizing
Tint SPF 30+

FAIR

FACIAL SUNSCREEN

50 mL / 1.7 fl. oz. e

Principal Display Panel - 50mL Carton Label

MOISTURIZING TINT SPF 30
octinoxate, octisalate, oxybenzone, avobenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:60541-0706
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	7.5 g in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	5 g in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y)	Oxybenzone	4 g in 1 mL
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	3 g in 1 mL

Ingredient Name	Strength
Inactive Ingredients
Water (UNII: 059QF0KO0R)
Isoeicosane (UNII: AR294KAG3T)
Potassium Cetyl Phosphate (UNII: 03KCY6P7UT)
Cetostearyl Alcohol (UNII: 2DMT128M1S)
Cetyl Dimethicone 45 (UNII: IK315POC44)
Dimethicone (UNII: 92RU3N3Y1O)
Ethylhexyl Methoxycrylene (UNII: S3KFG6Q5X8)
Glycerin (UNII: PDC6A3C0OX)
Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer (45000 Mpa.S At 1%) (UNII: 86FQE96TZ4)
Silicon Dioxide (UNII: ETJ7Z6XBU4)
Sorbitan Sesquioleate (UNII: 0W8RRI5W5A)
Isohexadecane (UNII: 918X1OUF1E)
Phenoxyethanol (UNII: HIE492ZZ3T)
Caprylyl Glycol (UNII: 00YIU5438U)
Ethylhexylglycerin (UNII: 147D247K3P)
Polysorbate 60 (UNII: CAL22UVI4M)
Hexylene Glycol (UNII: KEH0A3F75J)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Titanium Dioxide (UNII: 15FIX9V2JP)
Ferric Oxide Red (UNII: 1K09F3G675)

#	Item Code	Package Description
Packaging
1	NDC:60541-0706-7	1 in 1 BOX
1		50 mL in 1 BOTTLE

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	03/01/2014

Labeler - Hayden Caleel LLC (011367468)

Name	Address	ID/FEI	Business Operations
Establishment
Hayden Caleel LLC		011367468	MANUFACTURE(60541-0706)