Original Pain Relief Cream

Product NDC
69594-004
11-digit product format
695940004
Labeler code
69594
Product ID
69594-004_412d447f-56dc-4f62-8e5d-e4ce38bd0de8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Eucalyptus Oil and Tea Tree Oil
Dosage form
CREAM
Route
TOPICAL
Labeler
Ultra Mix (Aust) Pty Ltd
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2015-02-16
Marketing end
0000-00-00
Substance
EUCALYPTUS OIL; TEA TREE OIL
Active strength
39 mg/g; mg/g
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69594-004-012020-01-31C16284748780-19d75b9d1-099c-f424-e053-dadaa90a57ceOriginal Pain Relief Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69594-004-01Original Pain Relief Cream100 g in 1 TUBECREAM1001

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69594-004ORIGINAL PAIN RELIEF CREAM (EUCALYPTUS OIL AND TEA TREE OIL) CREAM [ULTRA MIX (AUST) PTY LTD ]1Legacy NDC, 1 package rows20150217_98572928-c809-48f6-9597-6105e2e6ed61.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69594-004-0169594000401100 g in 1 TUBE100 gHistorical