CNP LABORATORY SUN CARE MILKY LIGHT SUNSCREEN BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene cream

CNP Laboratory Sun Care Milky Light Sunscreen Broad Spectrum SPF 50 by

Drug Labeling and Warnings

CNP Laboratory Sun Care Milky Light Sunscreen Broad Spectrum SPF 50 by is a Otc medication manufactured, distributed, or labeled by fmg Co.Ltd, LG H&H Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Avobenzone 2.7%
Homosalate 9.0%
Octisalate 4.5%
Octocrylene 9.0%

PURPOSE

Sunscreen

USES

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

WARNINGS

For external use only

DO NOT USE

Do not use ​on damaged or broken skin

WHEN USING

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

STOP USE

Stop use and ask doctor if rash occurs

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.

DIRECTIONS

For sunscreen use:

• apply liberally 15 minutes before sun exposure
• children under 6 months of age: ask a doctor
• reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating
• 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 including:

- limit time in the sun, especially from 10 a.m. - 2 p.m.

- wear long-sleeved shirts, pants, hats, and sunglasses

OTHER INFORMATION

• protect the product in this container from excessive heat and direct sun
• the product may stain certain types of fabrics

INACTIVE INGREDIENTS

WATER, GLYCERIN, DIMETHICONE, CETEARYL ALCOHOL, ISODODECANE, POTASSIUM CETYL PHOSPHATE, ACRYLATES/POLYTRIMETHYLSILOXYMETHACRYLATE COPOLYMER, 1,2-HEXANEDIOL, BENZOTRIAZOLYL DODECYL P-CRESOL, PANTHENOL, GLYCERYL CAPRYLATE, GLYCERYL STEARATE, NIACINAMIDE, CAPRYLIC/CAPRIC TRIGLYCERIDE, MAGNESIUM ALUMINUM SILICATE, CETEARYL OLIVATE, INULIN LAURYL CARBAMATE, FRAGRANCE, SORBITAN OLIVATE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, XANTHAN GUM, DIPROPYLENE GLYCOL, TROMETHAMINE, TRISODIUM EDTA, MYRISTICA FRAGRANS (NUTMEG) EXTRACT, PAEONOL, PAEONIA SUFFRUTICOSA BRANCH/FLOWER/LEAF EXTRACT.

QUESTIONS?

www.cnpmall.com

+ Dermatologically tested

+ Dermatologically tested

This sunsreen delivers superior
broad spectrum protection against
harmful UVB and UVA rays and
provides skin care benefits. It con-
tains panthenol and niacinamide,
providing a moisturizing effect on
the skin and helping to brighten
the complexion. This lightweight
formula is absorbed without any
stickiness. Wear alone or under
makeup.

Questions?
www.cnpmall.com

MADE IN KOREA
DISTR. LG H&H Co., Ltd.
58, Saemunan-ro, Jongno-gu,
Seoul, Korea

PRINCIPAL DISPLAY PANEL 50ml / 1.7 fl. oz Tube Carton

CNP Laboratory

SUN CARE

MILKY
LIGHT
SUNSCREEN

Broad Spectrum
SPF 50

50 ml / 1.7 fl. oz

INGREDIENTS AND APPEARANCE

CNP LABORATORY SUN CARE MILKY LIGHT SUNSCREEN BROAD SPECTRUM SPF 50 
avobenzone, homosalate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72330-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 50 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	9 g  in 50 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2.7 g  in 50 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	9 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72330-101-50	1 in 1 CARTON	02/16/2024
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	02/16/2024

Labeler - fmg Co.Ltd (690188305)

Registrant - LG H&H Co.,Ltd. (688276187)

Establishment
Name	Address	ID/FEI	Business Operations
fmg Co.Ltd		690188305	manufacture(72330-101)