JER MOISTURIZING AND TRANSLUCENT SUNSCREEN lotion

JER Moisturizing and translucent sunscreen by

Drug Labeling and Warnings

JER Moisturizing and translucent sunscreen by is a Otc medication manufactured, distributed, or labeled by Guangdong Dayi Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

active ingredient

Octocrylene
Ethylhexyl Salicylate
Butyl Methoxydibenzoylmethane

Inactive ingrendient

beta-glucan
water
behenyl alcohol
arachidyl glucoside
arachidyl alcohol、
isononylisononanoate、
disiloxane、
arginine、
phenoxyethanol、

Purpose

SPF50 high-factor sunprotection, isolating UVA/UVB ultravioletrays, lightweight and easy to apply, forminginvisible protective net on the skin surface,resisting photoaging, and protecting the skinfrom ultraviolet damage,. Contains a varietyof plant extracts, which nourish and moisturthe skin while providing protection, leavingthe skin delicate and smooth,.

Warning

Ask a doctor before use if you haveSkin sensitization.Skin plastic surgery

Stop use

Ask a doctor before use if you haveSkin sensitization.Skin plastic surgery

keep out of reach of children

keep out of reach of children

Indication

How to use: After cleaning and toning, takean appropriate amount of this product andevenly apply it to the face, neck, hands, legsand back skin; it is best to apply it 20minutes before going out, To ensure the sunprotection effect, it is recommended toreapply it every hours.

Dosage

How to use: After cleaning and toning, takean appropriate amount of this product andevenly apply it to the face, neck, hands, legsand back skin; it is best to apply it 20minutes before going out, To ensure the sunprotection effect, it is recommended toreapply it every hours.

WHEN USING

it is best to apply it 20minutes before going out, To ensure the sunprotection effect, it is recommended toreapply it every hours.

85030-001-01

INGREDIENTS AND APPEARANCE

JER MOISTURIZING AND TRANSLUCENT SUNSCREEN 
jer moisturizing and translucent sunscreen lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85030-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2.5 g  in 50 g
ETHYLHEXYL SALICYLATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	ETHYLHEXYL SALICYLATE	2.5 g  in 50 g
BUTYL METHOXYDIBENZOYLMETHANE (UNII: G63QQF2NOX) (BUTYL METHOXYDIBENZOYLMETHANE - UNII:G63QQF2NOX)	BUTYL METHOXYDIBENZOYLMETHANE	1.5 g  in 50 g

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
BEHENYL ALCOHOL (UNII: 9G1OE216XY)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
DISILOXANE (UNII: D7M4659BPU)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
ARGININE (UNII: 94ZLA3W45F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85030-001-01	50 g in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/01/2025

Labeler - Guangdong Dayi Biotechnology Co., Ltd. (624457422)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Dayi Biotechnology Co., Ltd.		624457422	label(85030-001) , manufacture(85030-001)