Mineral Aqua Cream

Product NDC
73101-002
11-digit product format
731010002
Labeler code
73101
Product ID
73101-002_a5e83461-34cc-2ea3-e053-2995a90a56f5
Type
HUMAN OTC DRUG
Nonproprietary name
Allantoin
Dosage form
LIQUID
Route
TOPICAL
Labeler
UNION PROFIT MEDICINE LIMITED
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-05-18
Marketing end
0000-00-00
Substance
ALLANTOIN
Active strength
1 g/100g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73101-002-012022-01-28C16284748780-1d6a99b39-c05a-a426-e053-dadaa90af4c2a5e83461-34cb-2ea3-e053-2995a90a56f5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73101-002-01Mineral Aqua Cream120 g in 1 BOTTLELIQUID1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73101-002MINERAL AQUA CREAM (ALLANTOIN) LIQUID [UNION PROFIT MEDICINE LIMITED]1Legacy NDC, 1 package rows20200518_a5e83461-34cb-2ea3-e053-2995a90a56f5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73101-002-0173101000201120 g in 1 BOTTLE (73101-002-01) 120 g2020-05-180000-00-00NoNoCurrent