Advanced Relief A and D

Product NDC
42213-375
11-digit product format
422130375
Labeler code
42213
Product ID
42213-375_361c5383-24e2-4dbe-aa86-f540c576302c
Type
HUMAN OTC DRUG
Nonproprietary name
Petrolatum
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Ultra Seal Corporation
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2011-12-01
Marketing end
0000-00-00
Substance
PETROLATUM
Active strength
938 mg/g
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
42213-375-472023-12-05C16284748780-1f386c64a-20ae-0266-e053-dadaa90a7c1a7d6166ad-2227-4f9b-b6da-b85a6e124d75
42213-375-472023-01-30C16284748780-1f386c64a-20ae-0266-e053-dadaa90a7c1a7d6166ad-2227-4f9b-b6da-b85a6e124d75

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
42213-375-4742213037547144 PACKET in 1 CARTON (42213-375-47) > 5 g in 1 PACKET (42213-375-05) 144 packet2011-12-010000-00-00NoNoCurrent