PORE CARE Lotus Mask

Product NDC
71694-0001
11-digit product format
716940001
Labeler code
71694
Product ID
71694-0001_7aa98b05-0355-bdba-e053-2991aa0ae3ae
Type
HUMAN OTC DRUG
Nonproprietary name
Allantoin
Dosage form
LIQUID
Route
TOPICAL
Labeler
Feelxo
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2017-08-01
Marketing end
0000-00-00
Substance
ALLANTOIN
Active strength
0 g/100mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71694-0001-12020-01-31C16284748780-19d75b9d0-9145-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71694-0001-1PORE CARE Lotus Mask25 mL in 1 POUCHLIQUID252

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71694-0001PORE CARE LOTUS MASK (ALLANTOIN) LIQUID [FEELXO]2Legacy NDC, 1 package rows20181115_57de50d3-c9f6-5576-e053-2a91aa0a7937.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
71694-0001-17169400010125 mL in 1 POUCH25 mlHistorical