FDA.reportPublic FDA data

ZERO HOCL

Product NDC
76895-030
11-digit product format
768950030
Labeler code
76895
Product ID
76895-030_43f70d24-bbd1-45e8-a1c1-678a7212b4a1
Type
HUMAN OTC DRUG
Nonproprietary name
Hypochlorous Acid
Dosage form
GEL
Route
TOPICAL
Labeler
Lizcos Co.,Ltd.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2020-04-01
Marketing end
0000-00-00
Substance
HYPOCHLOROUS ACID
Active strength
495 g/500mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct76895-030DDiscontinued by firm2026-07-31
excluded packagepackage76895-03076895-030-01DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76895-030-0176895003001500 mL in 1 BOTTLE, PUMP (76895-030-01) 500 ml2020-04-010000-00-00NoNoCurrent