Eye Lubricant

Product NDC
37808-637
Requested package NDC
37808-637-05
11-digit product format
378080637
Labeler code
37808
Product ID
37808-637_b6752b96-4afc-7798-e053-2a95a90a154f
Type
HUMAN OTC DRUG
Nonproprietary name
polyethylene glycol, propylene glycol
Dosage form
LIQUID
Route
OPHTHALMIC
Labeler
H E B
Application
part349
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2012-12-05
Marketing end
0000-00-00
Substance
POLYETHYLENE GLYCOL 400; PROPYLENE GLYCOL
Active strength
4 mg/15mL; mg/15mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
37808-637-052020-04-24C16284748780-19d75b9cf-e441-f424-e053-dadaa90a57ceHEB Ultra Lubricant Eye Drops
37808-637-052020-01-31C16284748780-19d75b9cf-e441-f424-e053-dadaa90a57ceHEB Ultra Lubricant Eye Drops

DailyMed Socrata Ingredients#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37808-637-053780806370515 mL in 1 BOTTLE (37808-637-05) 15 ml2012-12-110000-00-00NoNoCurrent