ANUA INVISIBLE GLOW FINISH SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene stick

ANUA INVISIBLE GLOW FINISH SUNSCREEN by

Drug Labeling and Warnings

ANUA INVISIBLE GLOW FINISH SUNSCREEN by is a Otc medication manufactured, distributed, or labeled by The Founder Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Drug Facts

Active ingredient

Purpose

Other information

Directions

Uses

Warnings

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

Do not use

Do not use

• on damaged or broken skin

Stop use and ask a doctor if

Stop use and ask a doctor if

• rash occurs

When using this product

When using this product

• Keep out of eyes. Rinse with water to remove

Inactive ingredient

Questions

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANUA INVISIBLE GLOW FINISH SUNSCREEN 
avobenzone, homosalate, octisalate, octocrylene stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84610-300
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2.7 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	9.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
DIETHYLHEXYL CARBONATE (UNII: YCD50O0Z6L)
DIBUTYL LAUROYL GLUTAMIDE (UNII: 3V7K3IA58X)
WATER (UNII: 059QF0KO0R)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
DIMETHYLSILANOL HYALURONATE (UNII: Z853O1D4TE)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
DIBUTYL ETHYLHEXANOYL GLUTAMIDE (UNII: 0IAF2L30VS)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
CERAMIDE NP (UNII: 4370DF050B)
OCTYLDODECANOL (UNII: 461N1O614Y)
PANTHENOL (UNII: WV9CM0O67Z)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
HYALURONIC ACID (UNII: S270N0TRQY)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84610-300-01	17.5 g in 1 BOTTLE; Type 0: Not a Combination Product	11/14/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/14/2025

Labeler - The Founder Inc. (695015866)

Registrant - The Founder Inc. (695015866)