ZO MEDICAL SURFATROL Astringent

Product NDC
42851-084
11-digit product format
428510084
Labeler code
42851
Product ID
42851-084_af2e1f39-b312-41f4-923c-18a4dff99e1f
Type
HUMAN OTC DRUG
Nonproprietary name
Aluminum Acetate
Dosage form
POWDER
Route
TOPICAL
Labeler
ZO Skin Health, Inc.
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2016-08-01
Marketing end
0000-00-00
Substance
ALUMINUM ACETATE
Active strength
4866 mg/4.866g
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
42851-084-192023-08-01C16284748780-19d75b9cf-f476-f424-e053-dadaa90a57ce82f31fa8-960f-42c4-a0b1-9f91bad825b3
42851-084-192020-01-31C16284748780-19d75b9cf-f476-f424-e053-dadaa90a57ce82f31fa8-960f-42c4-a0b1-9f91bad825b3