SECRET DIG WHITENING SUNSCREEN SPRAY. SPF50 PA- secret dig whitening sunscreen spray spf50 pa aerosol, spray

Secret Dig Whitening Sunscreen Spray. SPF50 PA by

Drug Labeling and Warnings

Secret Dig Whitening Sunscreen Spray. SPF50 PA by is a Otc medication manufactured, distributed, or labeled by Yiwu Mijue electronic Commerce Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

HOMOSALATE

OCTINOXATE

OCTISALATE

PURPOSE

A lightweight sunscreen spray specially designed foroutdoor use can effectively block the exposure of UVA andUVB,evenly cover the skin, with fresh texture, and can breapplied at any time.lt is fresh and not greasy, and can formsunscreen isolation layer on the surface of the skin to providesunscreen care.

INDICATIONS & USAGE

A lightweight sunscreen spray specially designed for outdoor use can effectively block the exposure of UVA and UVB

Usage:Shake well before use,10-15cm away from the skin and spray evenly on the skin exposed to sunlight(hands,legs,neck,back)

DOSAGE & ADMINISTRATION

Store in a ventilated and dry environmen below 50 °c, avoid direct sunlight, and keep away from fire and heat sources.

Net:150ml

KEEP OUT OF REACH OF CHILDREN

Please keep out of reach of infants and young children

WARNINGS

Warning:For external use only,please do not ch e mouh,nose or eyes,do not use in areas with skin damage inflammation or itching

INACTIVE INGREDIENT

DECYL GLUCOSIDE

BISOCTRIZOLE

WATER

DEHYDROXANTHAN GUM

N-SALICYLOYLGLYCINE

BEMOTRIZINOL

ETHYLHEXYL TRIAZONE

2-PHENYLPROPANAL PROPYLENE GLYCOL ACETAL

OCTOCRYLENE

ZINC OXIDE

STEARIC ACID

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SECRET DIG WHITENING SUNSCREEN SPRAY. SPF50 PA 
secret dig whitening sunscreen spray spf50 pa aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84462-458
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	36 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	36 g  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	20 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
BISOCTRIZOLE (UNII: 8NT850T0YS)
WATER (UNII: 059QF0KO0R)
DEHYDROXANTHAN GUM (UNII: 63ZP7I1BQO)
N-SALICYLOYLGLYCINE (UNII: 5BR3P7J05U)
BEMOTRIZINOL (UNII: PWZ1720CBH)
ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
2-PHENYLPROPANAL PROPYLENE GLYCOL ACETAL (UNII: 1ZRR9A405A)
OCTOCRYLENE (UNII: 5A68WGF6WM)
ZINC OXIDE (UNII: SOI2LOH54Z)
STEARIC ACID (UNII: 4ELV7Z65AP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84462-458-01	150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/27/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	06/27/2024

Labeler - Yiwu Mijue electronic Commerce Co., LTD (413886387)

Establishment
Name	Address	ID/FEI	Business Operations
Yiwu Mijue electronic Commerce Co., LTD		413886387	manufacture(84462-458) , label(84462-458)