AMBI EVEN AND CLEAR FACIAL MOISTURIZER- homosalate 15%, octisalate 5%, octocrylene 3%, avobenzone 3% cream

Ambi Even and Clear Facial Moisturizer by

Drug Labeling and Warnings

Ambi Even and Clear Facial Moisturizer by is a Otc medication manufactured, distributed, or labeled by 73453-112, Paklab. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Homosalate 15%

Octisalate 5%

Octocrylene 3%

Avobenzone 3%

Purpose

Sunscreen

Uses

helps prevent sunburn. if used s directed with other sun protection measures (see Directions), decrease the risk of skin cancer and early skin aging caused by the sun.

Warnings

For external use only

Do not use on

do not use on damaged or broken skin

When using this product

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask

Stop use and ask a doctor if rash occurs

Keep out of reach of children

If swallowed, get medical attention or contact a Poison Control Center immediately

Directions

apply liberally 15-minutes before sun exposure. reapply at least every two hours. Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun proetection measures inlcuding: limit time in the sun, especially betwen 10am and 2pm. wear long sleeve shirts, pants, hats and sunglasses. for children under 6-months, consult a physician.

Other information:

protect this product from excessive heat and direct sunlight

Inactive ingredients:

water (aqua), glycerin, potassium cetyl phosphate, caprylic/capric triglyceride, squalane, cetearyl olivate, sorbitan olivate, cellulose, silica, phenoxyethanol, butyrospermum parkii (shea) butter, xanthan gum, carbomer, tocopherol, ethylhexylglycerin, camellia oleifera leaf extract, alo barbadensis leaf juice, trisodium ethylenediamine disuccinate, sodium hydroxide, ipomoea batatas root extract, plantago major leaf extract, sodium hyaluronate, ascorbyl palmitate, arctostaphylos uva-ursi leaf extract, glycyrrhiza glabra (licorice) root extract.

Questions or comments?

1-800-946-6354

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AMBI EVEN AND CLEAR FACIAL MOISTURIZER 
homosalate 15%, octisalate 5%, octocrylene 3%, avobenzone 3% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73453-112
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	15 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PLANTAGO MAJOR LEAF (UNII: 7DC28K241X)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
CARBOMER (UNII: 0A5MM307FC)
ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
GLYCYRRHIZA GLABRA (LICORICE) ROOT (UNII: 2788Z9758H)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
SQUALANE (UNII: GW89575KF9)
XANTHAN GUM (UNII: TTV12P4NEE)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
TOCOPHEROL (UNII: R0ZB2556P8)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
SORBITAN OLIVATE (UNII: MDL271E3GR)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
WATER (UNII: 059QF0KO0R)
CELLULOSE, OXIDIZED (UNII: 44AIH82TSC)
IPOMOEA BATATAS LEAF (UNII: FB3PS871YO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73453-112-02	1 in 1 BOX	12/22/2025
1		50 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/22/2025

Labeler - 73453-112 (117015229)

Establishment
Name	Address	ID/FEI	Business Operations
Paklab		177711082	manufacture(73453-112)