s panax all in one mist

Product NDC
81885-0002
11-digit product format
818850002
Labeler code
81885
Product ID
81885-0002_c293fb01-f74d-7e14-e053-2995a90a7c79
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium benzoate
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
SODIUM BENZOATE
Active strength
1 g/100mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81885-0002-1s panax all in one mist80 mL in 1 BOTTLELIQUID802

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81885-0002S PANAX ALL IN ONE MIST (SODIUM BENZOATE) LIQUID [S AND PANAX CO LTD]2Legacy NDC, 1 package rows20230215_c293e8b6-e178-345e-e053-2995a90ad0fd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
81885-0002-18188500020180 mL in 1 BOTTLE (81885-0002-1) 80 ml2021-05-180000-00-00NoNoCurrent