Benzoin Compound Tincture Professional Pack

Product NDC
0395-4209
11-digit product format
003954209
Labeler code
0395
Product ID
0395-4209_a8760d26-3891-ddd9-e053-2a95a90a2924
Type
HUMAN OTC DRUG
Nonproprietary name
Benzoin Resin
Dosage form
LIQUID
Route
TOPICAL
Labeler
Humco Holding Group, Inc.
Application
part356
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
1998-03-25
Marketing end
2020-09-30
Substance
BENZOIN RESIN
Active strength
1000 mg/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0395-4209-92ML - Milliliter0395-4209e65d4b74-a18b-4bd6-b28d-fed252825cf612014-04-03