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 W A 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

Citrullus Lanatus Seed oil, Flavor, Isopropyl myristate, Octyldodecanol, Phenoxyethanol, Polybutene, Sodium Benzoate

OTHER SAFETY INFORMATION

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

DOSAGE & ADMINISTRATION

Label

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: 30807-7000
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)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CITRULLUS LANATUS WHOLE (UNII: 3J5I6254YO)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)
OCTYLDODECANOL (UNII: 461N1O614Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30807-7000-1	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)