Sinus Wash Packet

Product NDC
11822-0474
11-digit product format
118220474
Labeler code
11822
Product ID
11822-0474_d5b44ae7-81e9-1413-e053-2995a90a5933
Type
HUMAN OTC DRUG
Nonproprietary name
SODIUM BICARBONATE, SODIUM CHLORIDE
Dosage form
POWDER
Route
NASAL
Labeler
RITE AID CORPORATION
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2022-01-16
Marketing end
0000-00-00
Substance
SODIUM BICARBONATE; SODIUM CHLORIDE
Active strength
23 mg/100mg; mg/100mg
Pharmacologic classes
Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-0474-3Sinus Wash Pre Mixed Ready to UseRite Aid3000 mg in 1 PACKETPOWDER3000 mg77.8 mg in 100mg7

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-0474-011822047400100 PACKET in 1 CARTON (11822-0474-0) > 3000 mg in 1 PACKET (11822-0474-1) 100 packet2022-01-160000-00-00NoNoCurrent
11822-0474-3118220474033000 mg in 1 PACKET3000 mgHistorical