UltraCare

Product NDC
51206-202
11-digit product format
512060202
Labeler code
51206
Product ID
51206-202_19052b2e-209d-4151-a35c-2ee002fb4fdb
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine
Dosage form
GEL
Route
DENTAL
Labeler
Ultradent Products, Inc.
Application
part356
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
1993-06-01
Marketing end
2024-12-31
Substance
BENZOCAINE
Active strength
200 mg/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51206-202-015120602020130 mL in 1 BOTTLE (51206-202-01) 30 ml1993-06-012023-01-08NoNoCurrent
51206-202-02512060202021 SYRINGE, PLASTIC in 1 BOX (51206-202-02) > 30 mL in 1 SYRINGE, PLASTIC1993-06-012024-12-31NoNoCurrent
51206-202-035120602020320 SYRINGE, PLASTIC in 1 PACKAGE (51206-202-03) > 1.2 mL in 1 SYRINGE, PLASTIC1993-06-012024-12-31NoNoCurrent
51206-202-045120602020450 SYRINGE, PLASTIC in 1 BAG (51206-202-04) > .4 mL in 1 SYRINGE, PLASTIC1993-06-012024-07-31NoNoCurrent
51206-202-05512060202051 SYRINGE, PLASTIC in 1 BAG (51206-202-05) > .4 mL in 1 SYRINGE, PLASTIC1993-06-012024-12-31NoNoCurrent