GLOW GO LIP OIL- avobenzone 30mg/g, homosalate 100mg/g, octocrylene 100mg/g, octisalate 50mg/g, oil

Glow Go Lip Oil by

Drug Labeling and Warnings

Glow Go Lip Oil by is a Otc medication manufactured, distributed, or labeled by WILD CHILD WA PTY LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

AVOBENZONE 3 %

HOMOSALATE 10%

OCTISALATE 5 %

OCTOCRYLENE 10%

PURPOSE

SUNSCREEN

USE

- Helps prevents sunburn

- If used as directed with other sun protection measures ( see directions) decreases the risk of skin cancer and early skin ageing caused by the sun.

WARNINGS

FOR EXTERNAL USE ONLY

- Do not use on damaged or broken skin.

WHEN USING

keep out of eyes, Rinse with water to remove

Stop use & ask doctor

If rash occurs

KEEP OUT OF REACH OF CHILDREN

If product is swallowed , get medical help or contact a poison control center right away

Directions

- Apply 20 minutes before sun exposure

- Use a water resistant sunscreen if swimming or sweating

- Re-apply frequently especially after swimming excercising or towel drying

- Re-apply 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 inclusing:

- limit time in the sun, especially from 10:00 AM- 02:00 PM

- Wear long- Sleeved shirts , pants, Hats and sunglasses

Inactive Ingredients

Inactive Ingredients: Candelilla Wax,
Citrullus Lanatus Seed Oil, Ethylhexylglycerin,
Flavor, Iron Oxides, Isopropyl Myristate, Mica,
Octyldodecanol, Phenoxyethanol, Polybutene,
Rubus Idaeus (Raspberry) Seed Oil, Silica,
Solanum Lycopersicum (Tomato) Fruit Extract

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat & direct sun

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GLOW GO LIP OIL 
avobenzone 30mg/g, homosalate 100mg/g, octocrylene 100mg/g, octisalate 50mg/g, oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 30807-8000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	10 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
MICA (UNII: V8A1AW0880)
POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)
CANDELILLA WAX (UNII: WL0328HX19)
CITRULLUS LANATUS WHOLE (UNII: 3J5I6254YO)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
OCTYLDODECANOL (UNII: 461N1O614Y)
TOMATO EXTRACT CONTAINING LYCOPENE (UNII: N53I4V2IA6)
RASPBERRY SEED OIL (UNII: 9S8867952A)
FERRIC OXIDE RED (UNII: 1K09F3G675)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30807-8000-1	4.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/07/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	08/07/2022

Labeler - WILD CHILD LABORATORIES PTY LTD (890661643)