BOTAO BABY MINERAL FOAM- zinc oxide lotion 
Peer Pharm Ltd.

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Botao Baby Mineral Foam Spray SPF 50

Drug Facts

Active Ingredients(in each 30 ml)

Zinc Oxide 24.5%

Purpose

Sunscreen

Uses

warnings

Do not use

  • on damaged or broken skin.

When using this product,

  • Keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

  • if rash or irritation develops and lasts.

Keep out of reach of children.

If swallowed, call a poison control center or get medical help right  away.

Directions

shake well before each use

spray liberally and spread evenly by hand 15 minutes before sun exposure

hold4 to 6 inches from the skin to apply

do not spray directly into face.

Spray on hands then apply to face

do not apply in windy conditions

Use in a well-ventilated area

reapply: after 40 minutes of swimming or sweating

immediately after towel drying

at least every 2 hours

Inactive Ingredients

Water,Coco-Caprylate, Styrene/Acrylates Copolymer,Butane,Isobutane, Propane, Octlydodecyl Citrate Crosspolymer,Cetearyl Olivate, Sorbitan Olivate, Caprylyl Glycol, Glycerin, Polyhydroxystearic acid, Aloe Barbadensis Leaf Juice, Panthenol, Triethoxycapryllsilane, Cetearyl Alcohol,Tocopherol, Butyrosperum Parkii (Shea) Butter,Silica, Silica Dimethyl Silyate , Xanthan Gum, Caprylhydroxamix Acid, Propanediol, Sodium Phytate, Dipotassium Glycyrrhizate, Chamomilla Recutita, (Matricaria) Flower Extract ,Calendula Officianlis Flower Extract,Citric Acid

Other Information

Package Labeling

baby

BOTAO BABY MINERAL FOAM 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69435-1503
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE24 g  in 96 g
Inactive Ingredients
Ingredient NameStrength
TOCOPHEROL (UNII: R0ZB2556P8)  
CITRIC ACID ISOPROPYL ETHER (UNII: 19776V0481)  
CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)  
HEXASODIUM PHYTATE (UNII: ZBX50UG81V)  
CALENDULA OFFICINALIS SEED OIL (UNII: 9JS8DS42SV)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
SHEA BUTTER (UNII: K49155WL9Y)  
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
DIPOTASSIUM GLUCOSE-6-PHOSPHATE (UNII: ZZW95F4360)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
COCO-CAPRYLATE (UNII: 4828G836N6)  
SODIUM ACRYLATE/STYRENE SULFONATE COPOLYMER (11000 MW) (UNII: N30934870L)  
ISOBUTANE (UNII: BXR49TP611)  
WATER (UNII: 059QF0KO0R)  
1-(ETHYLTRISULFANYL)PROPANE (UNII: 4SOS6O9G2X)  
TRIOCTYLDODECYL CITRATE (UNII: 35X8CT063R)  
ACRYLATES CROSSPOLYMER-4 (UNII: GEV2EL4D9G)  
CETEARYL OLIVATE (UNII: 58B69Q84JO)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
CASTOR OIL (UNII: D5340Y2I9G)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPANEDIOL 1-PHOSPHATE (UNII: 48G71659RB)  
CHAMOMILE (UNII: FGL3685T2X)  
PANTHENOL (UNII: WV9CM0O67Z)  
ALOE (UNII: V5VD430YW9)  
1,4-BUTANEDITHIOL (UNII: 7JD227IUMC)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69435-1503-196 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/19/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02005/19/2022
Labeler - Peer Pharm Ltd. (514678390)
Registrant - Peer Pharm Ltd. (514678390)
Establishment
NameAddressID/FEIBusiness Operations
Peer Pharm Ltd.514678390manufacture(69435-1503)

Revised: 2/2024
Document Id: 11b72198-4e54-02a0-e063-6394a90ad0bd
Set id: e1562f60-8047-4392-e053-2a95a90a8968
Version: 2
Effective Time: 20240219
 
Peer Pharm Ltd.