PURPOSE

Product NDC: 24208-001
11-digit product format: 242080001
Labeler code: 24208
Product ID: 24208-001_22f5cdc2-86cc-7dfd-e063-6394a90a539d
Type: HUMAN OTC DRUG
Nonproprietary name: Octinoxate, Octisalate and Oxybenzone
Dosage form: LOTION
Route: TOPICAL
Labeler: Bausch & Lomb Incorporated
Application: M018
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2013-10-07
Substance: OCTINOXATE; OCTISALATE; OXYBENZONE
Active strength: 7.5; 5; 3 g/100g; g/100g; g/100g
NDC exclude flag: No
Listing certified through: 2027-12-31
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: PURPOSE
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTINOXATE	7.5 g/100g
OCTISALATE	5 g/100g
OXYBENZONE	3 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4Y5P7MUD51	Internal UNII lookup
4X49Y0596W	Internal UNII lookup
95OOS7VE0Y	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
a1e14135-b8da-4cee-8c5b-1893572f4de4	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
24208-001-04	PURPOSE	113 g in 1 BOTTLE	LOTION	113		3
24208-001-04	PURPOSE	1 in 1 CARTON	LOTION	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
24208-001	PURPOSE (OCTINOXATE, OCTISALATE AND OXYBENZONE) LOTION [BAUSCH & LOMB INCORPORATED]	3	Current NDC, Legacy NDC, 2 package rows	20240927_a1e14135-b8da-4cee-8c5b-1893572f4de4.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 25 of 25 · 485 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
REFRESH Optive Mega-3	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80	Allergan, Inc.	c5f2b3f2-2071-45bd-a010-67f848bc0233	2022-06-30	Warnings	Exact identifier application number: M018
REFRESH P.M.	MINERAL OIL, PETROLATUM	Allergan, Inc.	24365d64-cd94-41cc-a7e1-033102d98114	2022-06-30	Warnings	Exact identifier application number: M018
REFRESH PLUS	CARBOXYMETHYLCELLULOSE SODIUM	Allergan, Inc.	0f6a4b4b-cde6-4518-84b5-ce997f1154a7	2022-06-28	Warnings	Exact identifier application number: M018
CIRCLE K sterile eye drops	TETRAHYDROZOLINE HCL	Lil' Drug Store Products, Inc.	2c0e106c-16f6-ff4e-e063-6294a90a7dbb	2018-07-30	Warnings	Exact identifier application number: M018
Lil Drug Store Sterile Eye Drops Redness Reliever	TETRAHYDROZOLINE HCL	Lil' Drug Store Products, Inc.	2c0ea35c-ac52-1043-e063-6394a90a061c	2018-04-30	Warnings	Exact identifier application number: M018

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
95OOS7VE0Y	OXYBENZONE	131-57-7	OXYBENZONE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
24208-001-04	24208000104	1 BOTTLE in 1 CARTON (24208-001-04) / 113 g in 1 BOTTLE	1 bottle	2013-10-07	0000-00-00	No	No	Current