s panax all in one liquidsoap

Product NDC
81885-0001
11-digit product format
818850001
Labeler code
81885
Product ID
81885-0001_c2937dff-2592-15fb-e053-2a95a90a7b46
Type
HUMAN OTC DRUG
Nonproprietary name
salt
Dosage form
LIQUID
Route
TOPICAL
Labeler
S AND PANAX CO LTD
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2021-05-18
Marketing end
0000-00-00
Substance
SEA SALT
Active strength
2 g/100mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81885-0001-1s panax all in one liquidsoap500 mL in 1 BOTTLELIQUID5002
81885-0001-2s panax all in one liquidsoap80 mL in 1 BOTTLELIQUID802

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81885-0001S PANAX ALL IN ONE LIQUIDSOAP (SALT) LIQUID [S AND PANAX CO LTD]2Legacy NDC, 2 package rows20230215_c2937d47-e1aa-155a-e053-2a95a90a51a2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
81885-0001-181885000101500 mL in 1 BOTTLE (81885-0001-1) 500 ml2021-05-180000-00-00NoNoCurrent
81885-0001-28188500010280 mL in 1 BOTTLE (81885-0001-2) 80 ml2021-05-180000-00-00NoNoCurrent