Drs. pharmacy sunscreen SPF 30

Product NDC: 80489-232
11-digit product format: 804890232
Labeler code: 80489
Product ID: 80489-232_3134c223-e292-e2e6-e063-6294a90a7cfb
Type: HUMAN OTC DRUG
Nonproprietary name: sunscreen SPF 30
Dosage form: LOTION
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 30
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTISALATE	5 g/100g
HOMOSALATE	10 g/100g
AVOBENZONE	3 g/100g
OCTOCRYLENE	10 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4X49Y0596W	Internal UNII lookup
V06SV4M95S	Internal UNII lookup
G63QQF2NOX	Internal UNII lookup
5A68WGF6WM	Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
052dea5d-a775-8dc2-e063-6294a90a4f19	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
80489-232-01	Drs. pharmacy sunscreen SPF 30	133 g in 1 TUBE	LOTION	133	4
80489-232-02	Drs. pharmacy sunscreen SPF 30	118 g in 1 TUBE	LOTION	118	4
80489-232-03	Drs. pharmacy sunscreen SPF 30	85 g in 1 TUBE	LOTION	85	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80489-232	DRS. PHARMACY SUNSCREEN SPF 30 (SUNSCREEN SPF 30) LOTION [OL PHARMA TECH LLC. (DRS. PHARMACY)]	4	Current NDC, 3 package rows	20250330_052dea5d-a775-8dc2-e063-6294a90a4f19.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 326 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PARURE GOLD SKIN MATTE FOUNDATION NO-TRANSFER HIGH PERFECTION 24H CARE AND WEAR INFUSED WITH 24K GOLD AND WHITE PEONY WITH SUNSCREEN BROADSPECTRUM SPF 15 3W	OCTISALATE, TITANIUM DIOXIDE	Guerlain	15fe0429-720c-4975-953d-285aa7ee12ce	2023-11-08	Warnings	Exact identifier application number: M020
PARURE GOLD SKIN MATTE FOUNDATION NO-TRANSFER HIGH PERFECTION 24H CARE AND WEAR INFUSED WITH 24K GOLD AND WHITE PEONY WITH SUNSCREEN BROADSPECTRUM SPF 15 4W	OCTISALATE, TITANIUM DIOXIDE	Guerlain	1a733548-75a4-41ec-8d8d-3e6e9aad52e0	2023-11-08	Warnings	Exact identifier application number: M020
PARURE GOLD SKIN MATTE FOUNDATION NO-TRANSFER HIGH PERFECTION 24H CARE AND WEAR INFUSED WITH 24K GOLD AND WHITE PEONY WITH SUNSCREEN BROADSPECTRUM SPF 15 8N	OCTISALATE, TITANIUM DIOXIDE	Guerlain	f43c867a-161f-47b7-b3d8-7f7e6c672804	2023-11-08	Warnings	Exact identifier application number: M020
Aruba Sun SPF 70 Sunscreen	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Derma Care Research Labs, LLC	d96b4233-6d52-7621-e053-2a95a90a1b60	2023-11-08	Warnings	Exact identifier application number: M020
PARURE GOLD SKIN MATTE FOUNDATION NO-TRANSFER HIGH PERFECTION 24H CARE AND WEAR INFUSED WITH 24K GOLD AND WHITE PEONY WITH SUNSCREEN BROADSPECTRUM SPF 15 0C	OCTISALATE, TITANIUM DIOXIDE	Guerlain	0d75be99-7607-4964-bb6e-3c731644ab4e	2023-11-08	Warnings	Exact identifier application number: M020
Dead Sea Natural Face Moisturizer Broad Spectrum SPF 20	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	AHAVA Dead Sea Laboratories Ltd	dee4bdb8-5c6f-42f6-b15c-d109cd2d3140	2023-11-08	Warnings	Exact identifier application number: M020
Mineral Radiance Energizing Day BS SPF 15	AVOBENZONE, HOMOSALATE, AND OCTISALATE	AHAVA Dead Sea Laboratories Ltd	4cb8b21c-7727-441a-9d61-c90d79ac45dc	2023-11-08	Warnings	Exact identifier application number: M020
Jack Black Intense Therapy Lip Balm Passion Fruit	AVOBENZONE, OCTINOXATE LIP BALM SUNSCREEN	Jack Black, LLC	f34beb68-e5dc-45c4-a6d1-e9a031016228	2023-11-08	Warnings	Exact identifier application number: M020
Private Label SPF45 Water Resistant Paraben Free Sunscreen	OCTINOXATE, OCTISALATE, ZINC OXIDE SUNSCREEN	Swiss-American CDMO, LLC	f997f4fc-7da5-433c-9a53-2030b489b4f6	2023-11-07	Warnings	Exact identifier application number: M020
Private Label Moisturizing Oil Free Paraben Free SPF43	SUNSCREEN	Swiss-American CDMO, LLC	003e4221-f9d9-47c4-b10b-9876046b931a	2023-11-07	Warnings	Exact identifier application number: M020
AHAVA ACTIVE DEADSEA MINERALS TIME TO ENERGIZE AGE CONTROL MOISTURIZING BROAD SPECTRUM SPF15	AVOBENZONE, OCTISALATE, AND OCTOCRYLENE	AHAVA Dead Sea Laboratories Ltd	5a9ec221-a9ec-4473-8fb0-83f10ae775e2	2023-11-07	Warnings	Exact identifier application number: M020
Private Label Super Light Oil-Free SPF45	2.75% OCTINSALATE, 7.50% OCTINOXATE, 8.00% ZINC OXIDE SUNSCREEN	Swiss-American CDMO, LLC	6a08448a-46bc-4330-ae2d-f716bb4edfa7	2023-11-07	Warnings	Exact identifier application number: M020
GOLD MOUNTAIN BEAUTY Collagen Broad Spectrum SPF 30	OCTINOXATE, OCTISALATE, ZINC OXIDE	TT Fitness, Inc	617ef3af-4203-4664-b714-1b5fab2e0ee6	2023-11-06	Warnings	Exact identifier application number: M020
SEAWEED BATH CO. Clear Moisture Mineral SPF-30	ZINC OXIDE	The Seaweed Bath Co.	c241261c-d887-4ac2-89ce-93dcc0fce267	2023-11-06	Warnings	Exact identifier application number: M020
JESS BEAUTY Let It Sun Sunscreen SPF-50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	JESS BEAUTY PRODUCTS LLC	88628c11-dbc7-4404-9701-7944a685a13d	2023-11-06	Warnings	Exact identifier application number: M020
SEAWEED BATH CO. Sheer Mineral Sensitive SPF-50	ZINC OXIDE	The Seaweed Bath Co.	fdcfc7eb-da33-4461-a4f9-fe97ea6b873f	2023-11-06	Warnings	Exact identifier application number: M020
SANTO REMEDIOS Piel Eterna Radiance Sunscreen Primer SPF-42	TITANIUM DIOXIDE, ZINC OXIDE	SANTO REMEDIO LLC	82d210bc-b7ca-4d74-be58-85f175a75058	2023-11-06	Warnings	Exact identifier application number: M020
CALIFORNIA MANGO SPF-50 SUNSCREEN	AVOBENZONE, OCTISALATE, OCTOCRYLENE	CALMANGO, INC	183e523a-93ee-47ec-8bd4-5557af449ea5	2023-11-06	Warnings	Exact identifier application number: M020
Mineral Sunscreen SPF-30	TITANIUM DIOXIDE, ZINC OXIDE	NEWCO LLC	fa3c73a3-0dfb-4673-822a-45d946dee260	2023-11-06	Warnings	Exact identifier application number: M020
JESS BEAUTY Sun Drops Sunscreen Oil SPF-50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	JESS BEAUTY PRODUCTS LLC	4e05e9d6-5127-44ca-a331-3004b2ddb534	2023-11-06	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
80489-232-01	80489023201	133 g in 1 TUBE (80489-232-01)	133 g	2024-01-01	No	No	Current
80489-232-02	80489023202	118 g in 1 TUBE (80489-232-02)	118 g	2024-01-01	No	No	Current
80489-232-03	80489023203	85 g in 1 TUBE (80489-232-03)	85 g	2025-03-26	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drs. pharmacy sunscreen SPF 30	OL PHARMA TECH LLC. (Drs. Pharmacy) \| OL PHARMA TECH LLC. \| OL PHARMA TECH LLC., (Drs. Pharmacy)	2025-03-25	HUMAN OTC DRUG LABEL	4