innisfree Daily UV Defense Sunscreen

Product NDC
71220-086
11-digit product format
712200086
Labeler code
71220
Product ID
71220-086_440a2be6-c7f8-c9aa-e063-6394a90ac31d
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, and Octisalate Lotion
Dosage form
LOTION
Route
TOPICAL
Labeler
Innisfree Corporation
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-02-01
Marketing end
2027-09-17
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE
Active strength
1.25; 3.5; 2.15 g/50mL; g/50mL; g/50mL
NDC exclude flag
No
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
innisfree Daily UV Defense Sunscreen

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE1.25 g/50mL
HOMOSALATE3.5 g/50mL
OCTISALATE2.15 g/50mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
G63QQF2NOXInternal UNII lookup
V06SV4M95SInternal UNII lookup
4X49Y0596WInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
0e9b6697-28a3-f69f-e063-6394a90a9d11Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71220-086-08innisfree Daily UV Defense Sunscreen1 in 1 BOXLOTION16
71220-086-08innisfree Daily UV Defense Sunscreen50 mL in 1 TUBELOTION506
71220-086-40innisfree Daily UV Defense Sunscreen1 in 1 BOXLOTION16
71220-086-40innisfree Daily UV Defense Sunscreen100 mL in 1 TUBELOTION1006
71220-086-41innisfree Daily UV Defense Sunscreen1 in 1 BOXLOTION16
71220-086-41innisfree Daily UV Defense Sunscreen10 mL in 1 TUBELOTION106
71220-086-99innisfree Daily UV Defense Sunscreen1 in 1 BOXLOTION16
71220-086-99innisfree Daily UV Defense Sunscreen25 mL in 1 TUBELOTION256

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71220-086INNISFREE DAILY UV DEFENSE SUNSCREEN (AVOBENZONE, HOMOSALATE, AND OCTISALATE LOTION) LOTION [INNISFREE CORPORATION]5Current NDC, 8 package rows20241105_0e9b6697-28a3-f69f-e063-6394a90a9d11.zip

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 120 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Tinted Mineral SunscreenTITANIUM DIOXIDE, ZINC OXIDEESTHETICS BY RIKI LLC387d5194-bc12-68c1-e063-6394a90ab1522025-12-15Exact identifier
application number: M020
Tinted Mineral Sun ProtectantTITANIUM DIOXIDE, ZINC OXIDEPANDA PAMPERING LLC387c23c2-a9f0-f484-e063-6394a90a41042025-12-15Exact identifier
application number: M020
Tinted Mineral Sun ProtectantTITANIUM DIOXIDE, ZINC OXIDEPANDA PAMPERING LLC387be96f-8cda-ce02-e063-6394a90abea52025-12-15Exact identifier
application number: M020
Serum Lightly TintedZINC OXIDEPANDA PAMPERING LLC387c593b-c65b-62b5-e063-6294a90ac4c22025-12-15Exact identifier
application number: M020
Serum Lightly TintedZINC OXIDEPANDA PAMPERING LLC387c9167-638c-1e30-e063-6394a90a93742025-12-15Exact identifier
application number: M020
REJUVN8TITANIUM DIOXIDE, ZINC OXIDEFLEUR DE VIE LLC37ede476-43b6-a7c8-e063-6294a90a3e8f2025-12-15Exact identifier
application number: M020
REJUVN8TITANIUM DIOXIDE, ZINC OXIDEFLEUR DE VIE LLC37efa5e1-e88e-d251-e063-6394a90a93712025-12-15Exact identifier
application number: M020
Non-Tinted Mineral SunscreenTITANIUM DIOXIDE, ZINC OXIDETHE BEAUTY ROOM OC INC3dd330bf-92e4-3664-e063-6294a90a04752025-12-15WarningsExact identifier
application number: M020
Tinted Mineral SunscreenTITANIUM DIOXIDE, ZINC OXIDETHE BEAUTY ROOM OC INC3dd37dd1-fd43-7af4-e063-6394a90ae3a02025-12-15WarningsExact identifier
application number: M020
Non-Tinted Mineral SunscreenTITANIUM DIOXIDE, ZINC OXIDETHE BEAUTY ROOM OC INC3dd3dcab-e9fb-0ef5-e063-6394a90acef12025-12-15WarningsExact identifier
application number: M020
Tinted Mineral SunscreenTITANIUM DIOXIDE, ZINC OXIDETHE BEAUTY ROOM OC INC3dd40a6a-d52e-ab87-e063-6294a90a966e2025-12-15WarningsExact identifier
application number: M020
20 Zinc Oxide Non-Tinted Mineral SunscreenZINC OXIDEAGELESS SKINCARE INC3766e6c0-8976-509d-e063-6394a90af00f2025-12-15Exact identifier
application number: M020
20 Zinc Oxide Tinted Mineral SunscreenZINC OXIDEAGELESS SKINCARE INC3766b00f-ceda-a6f9-e063-6294a90aff5d2025-12-15Exact identifier
application number: M020
Mattifying Skin PrimerTITANIUM DIOXIDE, ZINC OXIDESKIN MAVEN37662032-2842-1982-e063-6294a90a49a02025-12-15Exact identifier
application number: M020
Moisturizing Face and Body SPFZINC OXIDESKIN MAVEN376645ee-7ea8-e738-e063-6394a90a119b2025-12-15Exact identifier
application number: M020
Mermaid Glow And Go Non Tinted Mineral SunscreenZINC OXIDEMermaid Glow LLC3985a298-fe0b-c296-e063-6294a90ab6c02025-12-15Exact identifier
application number: M020
Mermaid Glow And Go Non Tinted Mineral SunscreenZINC OXIDEMermaid Glow LLC39856675-c110-a7a7-e063-6294a90ac6af2025-12-15Exact identifier
application number: M020
Bio H Plus Daily Defense And RevitalizeZINC OXIDEBIOHEALTH PLUS LLC3764f723-cc7a-2128-e063-6294a90ac8942025-12-15Exact identifier
application number: M020
Extreme Protection Non TintedZINC OXIDEBIOHEALTH PLUS LLC37656077-5185-817a-e063-6394a90adf5a2025-12-15Exact identifier
application number: M020
Deluxe Lip ProtectionTITANIUM DIOXIDE, ZINC OXIDEBIOHEALTH PLUS LLC37657895-5fec-82d0-e063-6294a90acf672025-12-15Exact identifier
application number: M020

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71220-086-08712200086081 TUBE in 1 BOX (71220-086-08) / 50 mL in 1 TUBE1 tube2024-02-012027-09-15NoNoHistorical
71220-086-40712200086401 TUBE in 1 BOX (71220-086-40) / 100 mL in 1 TUBE1 tube2024-07-012027-09-17NoNoHistorical
71220-086-41712200086411 TUBE in 1 BOX (71220-086-41) / 10 mL in 1 TUBE1 tube2024-07-012027-03-05NoNoHistorical
71220-086-99712200086991 TUBE in 1 BOX (71220-086-99) / 25 mL in 1 TUBE1 tube2024-07-012026-12-16NoNoHistorical