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Product NDC
54111-113
11-digit product format
541110113
Labeler code
54111
Product ID
54111-113_f2b36f8d-4de8-4e83-baa6-71fe2a7697f2
Type
HUMAN OTC DRUG
Nonproprietary name
ALLANTOIN
Dosage form
CREAM
Route
TOPICAL
Labeler
Bentley Laboratories, LLC
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2014-05-05
Marketing end
0000-00-00
Substance
ALLANTOIN
Active strength
0 g/85mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
54111-113-505411101135085 mL in 1 TUBE (54111-113-50) 85 ml2014-05-050000-00-00NoNoCurrent