Home NDC 29485-8158-6 24 / 7 Life Extra Strength Pain Reliever PM
Product NDC 29485-8158
Requested package NDC 29485-8158-6
11-digit product format 294858158
Labeler code 29485
Product ID 29485-8158_efa7d4de-8692-3fa2-e053-2995a90abb12
Type HUMAN OTC DRUG
Nonproprietary name acetaminophen, diphenhydramine hcl tablet, film coated
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Mechanical Servants LLC
Application part343
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-12-17
Marketing end 0000-00-00
Substance ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active strength 500 mg/1; mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 29485-8158 24 / 7 LIFE EXTRA STRENGTH PAIN RELIEVER PM (ACETAMINOPHEN, DIPHENHYDRAMINE HCL TABLET, FILM COATED) TABLET, FILM COATED [LIL' DRUG STORE PRODUCTS, INC.] 5 Legacy NDC 20241101_efa7d4de-8691-3fa2-e053-2995a90abb12.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 29485-8158-6 29485815806 6 BLISTER PACK in 1 CARTON (29485-8158-6) > 6 TABLET, FILM COATED in 1 BLISTER PACK 6 blister pack 2020-12-17 0000-00-00 No No Current