FDA.reportPublic FDA data

Drs. pharmacy sunscreen SPF 70

Product NDC
80489-234
11-digit product format
804890234
Labeler code
80489
Product ID
80489-234_3134fb87-407c-0da5-e063-6294a90a779c
Type
HUMAN OTC DRUG
Nonproprietary name
sunscreen SPF 70
Dosage form
CREAM
Route
TOPICAL
Labeler
OL PHARMA TECH LLC. (Drs. Pharmacy)
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-01-01
Substance
OCTISALATE; HOMOSALATE; AVOBENZONE; OCTOCRYLENE
Active strength
5; 10; 3; 10 g/100g; g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
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
Drs. pharmacy sunscreen SPF 70
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTISALATE5 g/100g
HOMOSALATE10 g/100g
AVOBENZONE3 g/100g
OCTOCRYLENE10 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4X49Y0596WInternal UNII lookup
V06SV4M95SInternal UNII lookup
G63QQF2NOXInternal UNII lookup
5A68WGF6WMInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
0def6fa1-b028-fad5-e063-6394a90a1913Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80489-234-01Drs. pharmacy sunscreen SPF 70118 g in 1 TUBECREAM1183
80489-234-02Drs. pharmacy sunscreen SPF 7085 g in 1 TUBECREAM853

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80489-234DRS. PHARMACY SUNSCREEN SPF 70 (SUNSCREEN SPF 70) CREAM [OL PHARMA TECH LLC. (DRS. PHARMACY)]3Current NDC, 2 package rows20250330_0def6fa1-b028-fad5-e063-6394a90a1913.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 125 of 353 · 7,049 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Daily RestoreZINC OXIDETYRLIN ENTERPRISES, INC.35cead50-86a7-2cf2-e063-6294a90a5f992025-12-15Exact identifier
application number: M020
Daily Defense Facial Sunscreen Plus PrimerTITANIUM DIOXIDE, ZINC OXIDELAURA CATHERINE, LLC36e81e8e-0ba7-93e6-e063-6294a90a4e622025-12-15Exact identifier
application number: M020
Sacred AuraZINC OXIDEIRIA SKIN OASIS LLC36eaaa54-e288-6590-e063-6394a90a403d2025-12-15Exact identifier
application number: M020
Daily Defense Facial Sunscreen Plus PrimerTITANIUM DIOXIDE, ZINC OXIDELAURA CATHERINE, LLC36e84147-5dcd-517a-e063-6394a90a54ee2025-12-15Exact identifier
application number: M020
Sacred GlowZINC OXIDEIRIA SKIN OASIS LLC36ead65c-a46c-7395-e063-6394a90a9e042025-12-15Exact identifier
application number: M020
Sheer Mineral Face And Body Sunscreen Non TintedZINC OXIDELAURA CATHERINE, LLC36e91877-c4c4-7fa3-e063-6294a90a13262025-12-15Exact identifier
application number: M020
Sheer Mineral Face And Body Sunscreen TintedZINC OXIDELAURA CATHERINE, LLC36e880af-debc-657f-e063-6394a90ab6ff2025-12-15Exact identifier
application number: M020
Sheer Mineral Face And Body Sunscreen TintedZINC OXIDELAURA CATHERINE, LLC36e8b631-03e7-c1de-e063-6294a90aa5302025-12-15Exact identifier
application number: M020
Sheer Mineral Face And Body Sunscreen Non TintedZINC OXIDELAURA CATHERINE, LLC36e957cf-cfa5-b122-e063-6294a90a78ce2025-12-15Exact identifier
application number: M020
Skin Shield PlusZINC OXIDELAURA CATHERINE, LLC36e9c2f3-ea89-0de3-e063-6394a90a9fb62025-12-15Exact identifier
application number: M020
Skin Shield PlusZINC OXIDELAURA CATHERINE, LLC36e9958b-cc5c-f7ff-e063-6394a90ac80d2025-12-15Exact identifier
application number: M020
Tinted Mineral Sunscreen Plus Primer MatteTITANIUM DIOXIDE, ZINC OXIDESimply Bare Waxing & Skin Care LLC36d8e8ba-a3dd-257d-e063-6294a90a30d62025-12-15Exact identifier
application number: M020
Tinted Lip SunscreenTITANIUM DIOXIDE, ZINC OXIDELAURA CATHERINE, LLC36e9e8d7-3fcf-1e94-e063-6394a90a8dc62025-12-15Exact identifier
application number: M020
Tinted Mineral Sunscreen Plus Primer CPlusE GlowZINC OXIDESimply Bare Waxing & Skin Care LLC36d968df-5168-61bf-e063-6294a90a94b72025-12-15Exact identifier
application number: M020
Advanced Sun ProtectionTITANIUM DIOXIDE, ZINC OXIDEHELLO BEAUTIFUL SKIN STUDIO36d45b48-e08d-ef40-e063-6394a90a635c2025-12-15Exact identifier
application number: M020
Advanced Sun ProtectionTITANIUM DIOXIDE, ZINC OXIDEHELLO BEAUTIFUL SKIN STUDIO36d439fb-b9cf-2774-e063-6294a90ae8852025-12-15Exact identifier
application number: M020
Tinted Mineral Sunscreen Plus Primer CPlusE GlowZINC OXIDESimply Bare Waxing & Skin Care LLC36d9b48d-e3db-6ae2-e063-6294a90abbf52025-12-15Exact identifier
application number: M020
Tinted Mineral Sunscreen Plus Primer MatteTITANIUM DIOXIDE, ZINC OXIDESimply Bare Waxing & Skin Care LLC36d9d83b-7da7-a006-e063-6394a90a9d842025-12-15Exact identifier
application number: M020
Advanced Sun ProtectionTITANIUM DIOXIDE, ZINC OXIDEHELLO BEAUTIFUL SKIN & ACNE36d3ebc0-1de6-1998-e063-6294a90a02e62025-12-15Exact identifier
application number: M020
Sun Safe Lip BalmTITANIUM DIOXIDE, ZINC OXIDEREVIVE IN SOLANO36c4f0c9-5789-ca58-e063-6394a90a23232025-12-15Exact identifier
application number: M020

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
80489-234-0180489023401118 g in 1 TUBE (80489-234-01) 118 g2024-01-01NoNoCurrent
80489-234-028048902340285 g in 1 TUBE (80489-234-02) 85 g2024-01-01NoNoCurrent