Stomach Relief

Product NDC
0121-0910
11-digit product format
001210910
Labeler code
0121
Product ID
0121-0910_dec3f97d-3508-4672-e053-2a95a90a3df0
Type
HUMAN OTC DRUG
Nonproprietary name
Bismuth subsalicylate
Dosage form
LIQUID
Route
ORAL
Labeler
Pharmaceutical Associates, Inc.
Application
part335
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2020-07-17
Marketing end
0000-00-00
Substance
BISMUTH SUBSALICYLATE
Active strength
525 mg/30mL
Pharmacologic classes
Bismuth [CS], Bismuth [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0121-0910-30ML - Milliliter0121-0910e78c47fb-2e3a-4101-bed2-b07f44e4463312020-09-14
0121-0910-40ML - Milliliter0121-091050f66932-b743-4691-afc3-1ed8426dca8312020-09-14

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0121-0910-40001210910404 TRAY in 1 CASE (0121-0910-40) > 10 CUP, UNIT-DOSE in 1 TRAY > 30 mL in 1 CUP, UNIT-DOSE (0121-0910-30) 4 tray2020-07-172021-12-30NoNoCurrent