Label: BOTAO BABY MINERAL FOAM- zinc oxide lotion
- NDC Code(s): 69435-1503-1
- Packager: Peer Pharm Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 19, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients(in each 30 ml)
- Uses
- warnings
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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
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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
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INGREDIENTS AND APPEARANCE
BOTAO BABY MINERAL FOAM
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69435-1503 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 24 g in 96 g Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:69435-1503-1 96 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 05/19/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/19/2022 Labeler - Peer Pharm Ltd. (514678390) Registrant - Peer Pharm Ltd. (514678390) Establishment Name Address ID/FEI Business Operations Peer Pharm Ltd. 514678390 manufacture(69435-1503)