FDA.reportPublic FDA data

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
IngredientStrength
OCTINOXATE7.5 g/100g
OCTISALATE5 g/100g
OXYBENZONE3 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4Y5P7MUD51Internal UNII lookup
4X49Y0596WInternal UNII lookup
95OOS7VE0YInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
a1e14135-b8da-4cee-8c5b-1893572f4de4Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24208-001-04PURPOSE113 g in 1 BOTTLELOTION1133
24208-001-04PURPOSE1 in 1 CARTONLOTION13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24208-001PURPOSE (OCTINOXATE, OCTISALATE AND OXYBENZONE) LOTION [BAUSCH & LOMB INCORPORATED]3Current NDC, Legacy NDC, 2 package rows20240927_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 12 of 25 · 486 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Leader Lubricant Eye Drops Soothing ReliefCARBOXYMETHYLCELLULOSE SODIUMLEADER/Cardinal Health 110, Inc.218629d4-2704-a503-e063-6294a90a39532025-12-30WarningsExact identifier
application number: M018
Foster and Thrive Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUMStrategic Sourcing Services LLCfb85ebc0-1570-972b-e053-6294a90a3dc42025-12-30WarningsExact identifier
application number: M018
Archies Dry Eye ReliefPOLYETHYLENE GLYCOL 400, PROPYLENE GLYCOLArchie's Remedies07da099b-6b7f-984d-e063-6294a90a12ac2025-12-30WarningsExact identifier
application number: M018
Equate Optimal Hydration Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUM, GLYCERINWalmart, Inc.151b9723-5d5e-ac2b-e063-6294a90af0732025-12-30WarningsExact identifier
application number: M018
Equate Nighttime Relief LubricantLIGHT MINERAL OIL, WHITE PETROLATUMWalmart Inc.152171db-2f2a-9d36-e063-6394a90a72252025-12-30WarningsExact identifier
application number: M018
Equate Moisturizing Comfort Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUMWalmart Inc.152028bd-0429-720a-e063-6294a90a14652025-12-30WarningsExact identifier
application number: M018
Equaline Multi-Symptom Eye DropsPOLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATEUnited Natural Foods, Inc.fe467606-6d66-b695-e053-6294a90aab5d2025-12-30WarningsExact identifier
application number: M018
OCUFRESHWATEROptics Laboratory Inc.b8e477a9-66b9-496b-92fb-3d4bbd7b36b52025-12-29WarningsExact identifier
application number: M018
Kollourion Eyesalve EyewashPURIFIED WATER 98.3%Miracle Eye Pharmaceuticalsb56d2ab9-169b-b490-e053-2a95a90a80b32025-12-28WarningsExact identifier
application number: M018
Equate Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUM, GLYCERINHanlim46851e7c-8910-6456-e063-6394a90abafb2025-12-22WarningsExact identifier
application number: M018
Equate Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUMHanlim46854996-a0b9-46b4-e063-6294a90aa4332025-12-22WarningsExact identifier
application number: M018
Equate Nighttime Relief LubricantLIGHT MINERAL OIL, WHITE PETROLATUMHanlim Pharm Co. LTD468559a0-9586-9982-e063-6394a90af4662025-12-22WarningsExact identifier
application number: M018
Redness and Dry Eye ReliefGLYCERIN, NAPHAZOLINE HYDROCHLORIDEKC Pharmaceuticals, Inc4682f68d-6bdd-d860-e063-6394a90a2b522025-12-21WarningsExact identifier
application number: M018
Original Redness RelieverTETRAHYDROLIZINE HCLKC Pharmaceuticals4683b850-b0fc-5093-e063-6294a90aef442025-12-21WarningsExact identifier
application number: M018
Equate Nighttime Relief LubricantLIGHT MINERAL OIL, WHITE PETROLATUMWalmart4449a55b-2cd4-0cb9-e063-6294a90aafbc2025-12-20WarningsExact identifier
application number: M018
Equate Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUMWalmart44494842-e38d-617c-e063-6294a90afaf82025-12-20WarningsExact identifier
application number: M018
Equate Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUM, GLYCERINWalmart443e214b-2680-79a9-e063-6294a90a68ba2025-12-20WarningsExact identifier
application number: M018
Equate Redness and Dry Eye ReliefGLYCERIN, NAPHAZOLINE HYDROCHLORIDEWalmart44155cf8-6fd9-d16f-e063-6394a90ac7312025-12-20WarningsExact identifier
application number: M018
Original Redness RelieverTETRAHYDROLIZINE HCLWalmart4414f768-0c69-d041-e063-6294a90a5bd92025-12-20WarningsExact identifier
application number: M018
Walgreens LubricantPOLYETHYLENE GLYCOL 400, AND PROPYLENE GLYCOLWalgreens21dfe061-4538-2061-e063-6394a90a6e732025-12-19WarningsExact identifier
application number: M018

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
24208-001-04242080001041 BOTTLE in 1 CARTON (24208-001-04) / 113 g in 1 BOTTLE1 bottle2013-10-070000-00-00NoNoCurrent