GLIZA BODY MIST SUNSCREEN BROAD SPECTRUM SPF 100- sunscreen spray

GLIZA BODY MIST SUNSCREEN BROAD SPECTRUM SPF 100 by

Drug Labeling and Warnings

GLIZA BODY MIST SUNSCREEN BROAD SPECTRUM SPF 100 by is a Otc medication manufactured, distributed, or labeled by EMRA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Avobenzone 3% 
Homosalate 15% 
Octisalate 5% 
Octocrylene 10% 
Oxybenzone 6% 

Purpose

Sunscreen

Use

Uses helps prevent sunburn if used as  directed with other sun protection measures decreases the risk of skin cancer
and early skin aging caused by the sun.

Warnings

For External Use Only. Flammable, keep away from fire, sparks, and source of
ignition. Do not store above 110 oF

When using this product:

Keep out of eyes. In case of contact with eyes, ush thoroughly with water. Avoid contact
with broken skin.

Stop use and ask a doctor if irritation and redness develop and persist for more
than 72h.

Keep out of reach of children. If swallowed get medical help or contact a
Poison Control Centre immediately.

WHEN USING

Directions :

Spray liberally and spread evenly by hand 15 minutes before sun
exposur apply to all skin exposed to the sun. Reapply after 80 minutes of
swimming or sweating, immediately after towel drying. Reapply at least every
2 hours. Children under 6 months of age:
Ask a doctor

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Inactive ingredients

Ethyl Alcohol, Polyester-7 & Neopentyl Glycol Diheptanoate, Fragrance (Perfume),
Glycerine, Aloe Barbadensis Leaf Juice, Propanediol, Tocopherol (Vitamin E)
Phenoxyethanol, Ethylhexylglycerin,

Package Label - Principal Display Panel

0.06 L (60 mL) NDC: 77903-002-01

INGREDIENTS AND APPEARANCE

GLIZA BODY MIST SUNSCREEN BROAD SPECTRUM SPF 100 
sunscreen spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77903-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1.8 mg  in 60 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	9 mg  in 60 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	3 mg  in 60 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	6 mg  in 60 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	3.6 mg  in 60 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
POLYESTER (ADIPIC ACID, 1,6-HEXANEDIOL, NEOPENTYL GLYCOL) (UNII: 571593769G)
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPANEDIOL (UNII: 5965N8W85T)
TOCOPHEROL (UNII: R0ZB2556P8)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
2-ETHYLHEXYL GLYCIDYL ETHER (UNII: LU1UZ98B89)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77903-002-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/19/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	05/19/2020

Labeler - EMRA LLC (116584354)

Registrant - EMRA LLC (116584354)

Establishment
Name	Address	ID/FEI	Business Operations
EMRA LLC		116584354	manufacture(77903-002)