BLUME SUNBURST SUNSCREEN- zinc oxide lotion

Blume Sunburst Sunscreen by

Drug Labeling and Warnings

Blume Sunburst Sunscreen by is a Otc medication manufactured, distributed, or labeled by Blume. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Blume Sunburst Sunscreen

Blume Sunburst Sunscreen

Blume Sunburst Sunscreen

Blume Sunburst Sunscreen

Blume Sunburst Sunscreen

Blume Sunburst Sunscreen

Blume Sunburst Sunscreen

Blume Sunburst Sunscreen

INGREDIENTS AND APPEARANCE

BLUME SUNBURST SUNSCREEN 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83656-2106
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	132 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
FERROUS OXIDE (UNII: G7036X8B5H)
CENTELLA ASIATICA LEAF (UNII: 6810070TYD)
JOJOBA OIL (UNII: 724GKU717M)
ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TOCOPHEROL (UNII: R0ZB2556P8)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
COCO-CAPRYLATE (UNII: 4828G836N6)
NYLON-12 (UNII: 446U8J075B)
PHENYLPROPANOL (UNII: 0F897O3O4M)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
ALLANTOIN (UNII: 344S277G0Z)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O)
.ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
NIACINAMIDE (UNII: 25X51I8RD4)
PROPANEDIOL (UNII: 5965N8W85T)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
RUTIN (UNII: 5G06TVY3R7)

Product Characteristics
Color	brown	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83656-2106-2	1 in 1 CARTON	03/01/2024
1	NDC: 83656-2106-1	50 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/01/2024

Labeler - Blume (242110723)