BIO SPECTRA

Product NDC
61649-393
11-digit product format
616490393
Labeler code
61649
Product ID
61649-393_13f76dd5-ff47-407d-9bab-d564e97f85c1
Type
HUMAN OTC DRUG
Nonproprietary name
alcohol
Dosage form
SOLUTION
Route
TOPICAL
Labeler
BIO SPECTRA
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-11-15
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
72 mL/100mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61649-393-0161649039301100 mL in 1 BOTTLE, SPRAY (61649-393-01) 100 ml2020-11-150000-00-00NoNoCurrent
61649-393-0261649039302473 mL in 1 BOTTLE, PLASTIC (61649-393-02) 473 ml2020-11-150000-00-00NoNoCurrent