SUNSCREENSPRAY- sunscreen spray spray

SunscreenSpray by

Drug Labeling and Warnings

SunscreenSpray by is a Otc medication manufactured, distributed, or labeled by Guangzhou Kadiya Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Apply generously and evenly over wholebody 20 minutes before sun exposure.Reapply frequently

INACTIVE INGREDIENT

AQUA
MINERAL OIL
GLYCERIN
CETEARYL ALCOHOL
UREA
DIMETHICONE
GLYCERYL STEARATE
CETEARETH-20
POTASSIUM CETYL PHOSPHATE
PEG-100 STEARATE
TRIETHANOLAMINE
ALLANTOIN
CARBOMER
C13-16 ISOALKANE
DMDM HYDANTOIN
AROMA
METHYLPARABEN
PROPYLPARABEN
3-O-ETHYL ASCORBIC ACID
DISODIUM EDTA
BUTYLENE GLYCOL
IODOPROPYNYL BUTYLCARBAMATE
CI 19140

WARNINGS

1、For external use only, avoid contact with eyes when used
2、Keep out of reach of children

INDICATIONS & USAGE

Very high, broad spectrum protection for the body against UVA and UVB. Suitable for all skin types, especially those with very clear, sensitive phototypes and sun intolerance.

DOSAGE & ADMINISTRATION

Apply generously and evenly over whole body 20 minutes before sun exposure. Reapply frequently.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN SECTION

ACTIVE INGREDIENT

Active Ingredients
NIACINAMIDE1mg/
Zinc oxide6%

PRINCIPAL DISPLAY PANEL

Active Ingredients
NIACINAMIDE1mg/
Zinc oxide6%

Uses：
Apply generously and evenly over wholebody 20 minutes before sun exposure.Reapply frequently.
The storage method：
Store sealed in a cool place and out of sunlight

AQUA
MINERAL OIL
GLYCERIN
CETEARYL ALCOHOL

UREA
DIMETHICONE
GLYCERYL STEARATE
CETEARETH-20
POTASSIUM CETYL PHOSPHATE
PEG-100 STEARATE
TRIETHANOLAMINE
ALLANTOIN
CARBOMER
C13-16 ISOALKANE
DMDM HYDANTOIN
AROMA
METHYLPARABEN
PROPYLPARABEN
3-O-ETHYL ASCORBIC ACID
DISODIUM EDTA
BUTYLENE GLYCOL
IODOPROPYNYL BUTYLCARBAMATE
CI 19140

INGREDIENTS AND APPEARANCE

SUNSCREENSPRAY 
sunscreen spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84423-090
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	1 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	6 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CI 19140 (UNII: I753WB2F1M)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
C13-16 ISOPARAFFIN (UNII: LED42LZG6O)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
CETEARETH-20 (UNII: YRC528SWUY)
AQUA (UNII: 059QF0KO0R)
METHYLPARABEN (UNII: A2I8C7HI9T)
3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
ALLANTOIN (UNII: 344S277G0Z)
EDETATE DISODIUM (UNII: 7FLD91C86K)
MINERAL OIL (UNII: T5L8T28FGP)
UREA (UNII: 8W8T17847W)
TROLAMINE (UNII: 9O3K93S3TK)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
CARBOMER (UNII: 0A5MM307FC)
DMDM HYDANTOIN (UNII: BYR0546TOW)
PEG-100 STEARATE (UNII: YD01N1999R)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHICONE (UNII: 92RU3N3Y1O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84423-090-01	100 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/04/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/04/2025

Labeler - Guangzhou Kadiya Biotechnology Co., Ltd. (713172913)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Kadiya Biotechnology Co., Ltd.		713172913	manufacture(84423-090)