Sani-Care

Product NDC
63830-221
Requested package NDC
63830-221-28
11-digit product format
638300221
Labeler code
63830
Product ID
63830-221_785f1a4b-8d07-4446-8e9e-ca93535e046a
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
Pro Chem, Inc.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-07-16
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 mL/mL
NDC exclude flag
No
Listing certified through
2021-12-31
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 packagepackage63830-22163830-221-28DDiscontinued by firm2026-08-10

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 · 9 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26DDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31UExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20UExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90MSANI-CARE (ALCOHOL) GEL [PRO CHEM, INC.]2
ALCOHOLACTIVE MOIETY3K9958V90MSANI-CARE (ALCOHOL) GEL [PRO CHEM, INC.]2
.ALPHA.-TOCOPHEROL ACETATE, DL-INACTIVE INGREDIENTWR1WPI7EW8SANI-CARE (ALCOHOL) GEL [PRO CHEM, INC.]2
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XSANI-CARE (ALCOHOL) GEL [PRO CHEM, INC.]2
CARBOMER 934INACTIVE INGREDIENTZ135WT9208SANI-CARE (ALCOHOL) GEL [PRO CHEM, INC.]2
DIISOPROPYLAMINEINACTIVE INGREDIENTBR9JLI40NOSANI-CARE (ALCOHOL) GEL [PRO CHEM, INC.]2
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3SANI-CARE (ALCOHOL) GEL [PRO CHEM, INC.]2
WATERINACTIVE INGREDIENT059QF0KO0RSANI-CARE (ALCOHOL) GEL [PRO CHEM, INC.]2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63830-221-2863830022128149 mL in 1 BOTTLE, PLASTIC (63830-221-28) 149 ml2020-07-160000-00-00NoNoCurrent