TULIP DEW SUNSCREEN- zinc oxide lotion 
Bloomeffects, Inc.

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Tulip Dew Sunscreen

Drug Facts

Active Ingredient

Zinc Oxide 12%

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 & ask a doctor

  • if skin rash occurs.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive Ingredients:

Water (Aqua), C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Jojoba Esters, Tridecyl Salicylate, Propanediol, Polyglyceryl-4 Disostearate/Polyhydroxystearates/Sebacate, Niacinamide, Methylpropanediol, Silica, Nylon-12, Coco-Caprylate, Tulipa Gesneriana/Kaurmanniana Meristem Cell Lysate Filtrate Extract, Helianthus Annuus Extract, Glycerin, Sodium Hyaluronate, Sodium Lactate, Bisabolol, Allantoin, Oryza Sativa Bran Extract, Terminalia Ferdinandiana Fruit Extract, Podocarpus Elatus Fruit Extract, Pleiogynium Timoriense Fruit Extract, Lecithin, Hydrogenated Lecithin, Leuconostoc/Radish Root Ferment Filtrate, Rosmarinus Officinalis Leaf Extract, Sodium Chloride, Polyglyceryl-2 Dipolyhydroxystearate, Caprylyl Glycol, Methylheptyl Isostearate, Phenylpropanol, Tetrasodium Glutamate Diacetate, Sodium Gluconate, Pentylene Glycol, Sodium Hydroxide, Phenethyl Alcohol, Potassium Sorbate, Alcohol, Hamamelis Virginiana Water, Citric Acid, CI 77499, CI 77492, CI 77491.

Package Labeling:

Label

TULIP DEW SUNSCREEN 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82548-4530
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION120 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)  
PROPANEDIOL (UNII: 5965N8W85T)  
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)  
NIACINAMIDE (UNII: 25X51I8RD4)  
METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
NYLON-12 (UNII: 446U8J075B)  
COCO-CAPRYLATE (UNII: 4828G836N6)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
LEVOMENOL (UNII: 24WE03BX2T)  
ALLANTOIN (UNII: 344S277G0Z)  
KAKADU PLUM (UNII: 0ZQ1D2FDLI)  
PODOCARPUS ELATUS FRUIT (UNII: R4N1M6CZCY)  
PLEIOGYNIUM TIMORIENSE FRUIT (UNII: AF3VFG6MLV)  
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)  
ROSEMARY (UNII: IJ67X351P9)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
METHYLHEPTYL ISOSTEARATE (UNII: 981F40Q9FF)  
PHENYLPROPANOL (UNII: 0F897O3O4M)  
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
SODIUM GLUCONATE (UNII: R6Q3791S76)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
ALCOHOL (UNII: 3K9958V90M)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82548-4530-11 in 1 CARTON05/01/2022
155 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02005/01/2022
Labeler - Bloomeffects, Inc. (096991853)

Revised: 10/2023
Document Id: 081d934f-bbd7-0cea-e063-6394a90aac69
Set id: c7951aea-d9b2-4662-a0c2-b8604cffc5a4
Version: 3
Effective Time: 20231019
 
Bloomeffects, Inc.