FDA.reportPublic FDA data

Tulip Dew SHIELD GLOW

Manufacturer
Bloomeffects, Inc. | Inspec Solutions
Effective date
2025-07-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:08:24

Label at a glance#

ProductTulip Dew SHIELD GLOW
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Zinc Oxide 14.7%

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

WARNINGS SECTION

For external use only.

OTC - STOP USE SECTION

Stop use & ask a doctor if skin eash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center righ away.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Caprylic/Capric Triglyceride
Butyloctyl Salicylate
Butyrospermum Parkii(Shea) Oil
C12-15 Alkyl Benzoate
Dibutyl Ethylhexanoyl Glutamide
Dibutyl Lauroyl Glutamide
dl-alpha Tocopheryl Acetate
Ethylhexyl Methoxycrylene
Octyl Dodecanol
Phenoxyethanol
Propylene glycol
Simmondsia Chinenses Seed oil
Stevia Extract
Sodium hyaluronate
Triethoxycaprylylsilane
Tulipa Gesneriana Flower Extract
Vitis Vinifera (Grape) Seed Oil
VP/Hexadecene Copolymer
Water

OTC - PURPOSE SECTION

Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tulip dewtulip dew

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82548-2420-1Tulip Dew SHIELD GLOW17 g in 1 BOTTLE, PLASTICSTICK173

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82548-242082548-2420-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
SHEANUT OILO88E196QRFIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
DIBUTYL LAUROYL GLUTAMIDE3V7K3IA58XIACT
DIBUTYL ETHYLHEXANOYL GLUTAMIDE0IAF2L30VSIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
STEVIA REBAUDIUNA LEAF6TC6NN0876IACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
ETHYLHEXYL METHOXYCRYLENES3KFG6Q5X8IACT
JOJOBA OIL724GKU717MIACT
VINYLPYRROLIDONE/HEXADECENE COPOLYMERKFR5QEN0N9IACT
WATER059QF0KO0RIACT
2-HEXYLDODECANOLNR6259U734IACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
HYALURONATE SODIUMYSE9PPT4THIACT
GRAPE SEED OIL930MLC8XGGIACT
MAGNOLIA LILIIFLORA FLOWER BUDK99MFN37XXIACT
ZINC OXIDESOI2LOH54ZACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Tulip Dew SHIELD GLOWZINC OXIDEBloomeffects, Inc.150f9660-48ec-a189-e063-6294a90a6d492025-07-23WarningsExact identifier
ndc (package): 82548-2420-1
ndc (product): 82548-2420
ndc11 (package): 82548242001
spl id: 3a97e2bc-2458-309e-e063-6394a90a2480
spl set id: 150f9660-48ec-a189-e063-6294a90a6d49

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.