GNP Lubricating Relief

Product NDC
71205-084
11-digit product format
712050084
Labeler code
71205
Product ID
71205-084_c4f9017b-be83-4e8f-8826-cccd25c33f30
Type
HUMAN OTC DRUG
Nonproprietary name
Carboxymethylcellulose Sodium
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Proficient Rx LP
Application
part349
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2016-09-30
Marketing end
0000-00-00
Substance
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
Active strength
5 mg/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71205-084-15ML - Milliliter71205-084dbdc2c67-926f-4549-8767-94ad99a77d8212018-10-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71205-084-15712050084151 BOTTLE, DROPPER in 1 BOX (71205-084-15) > 15 mL in 1 BOTTLE, DROPPER2018-08-010000-00-00NoNoCurrent