Recens

Product NDC
75990-605
Requested package NDC
75990-605-27
11-digit product format
759900605
Labeler code
75990
Product ID
75990-605_eeb15c36-2fc6-1d6d-e053-2995a90aa4b3
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
Certus Medical, Inc.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-06-25
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 mL/mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage75990-60575990-605-27DDiscontinued by firm2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage75990-60575990-605-27DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage75990-60575990-605-27UExcluded because listing certification expiredexcluded / ndc_excluded.zip0efc9e666f02…f202fb6c5f17…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90MRECENS (ALCOHOL) GEL [CERTUS MEDICAL, INC.]2
ALCOHOLACTIVE MOIETY3K9958V90MRECENS (ALCOHOL) GEL [CERTUS MEDICAL, INC.]2
.ALPHA.-TOCOPHEROL ACETATE, DL-INACTIVE INGREDIENTWR1WPI7EW8RECENS (ALCOHOL) GEL [CERTUS MEDICAL, INC.]2
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XRECENS (ALCOHOL) GEL [CERTUS MEDICAL, INC.]2
CARBOMER 934INACTIVE INGREDIENTZ135WT9208RECENS (ALCOHOL) GEL [CERTUS MEDICAL, INC.]2
DIISOPROPYLAMINEINACTIVE INGREDIENTBR9JLI40NORECENS (ALCOHOL) GEL [CERTUS MEDICAL, INC.]2
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3RECENS (ALCOHOL) GEL [CERTUS MEDICAL, INC.]2
WATERINACTIVE INGREDIENT059QF0KO0RRECENS (ALCOHOL) GEL [CERTUS MEDICAL, INC.]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75990-605RECENS (ALCOHOL) GEL [CERTUS MEDICAL, INC.]10Legacy NDC20250114_839487e4-a036-4b00-8f42-4890e4165526.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
75990-605-2775990060527800 mL in 1 CARTRIDGE (75990-605-27) 800 ml2020-06-250000-00-00NoNoCurrent