alka-seltzer plus severe cough mucus and congestion day and night
Generic: acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, guaifenesin
Labeler: bayer healthcare llc.Drug Facts
Product Profile
Brand Name
alka-seltzer plus severe cough mucus and congestion day and night
Generic Name
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, guaifenesin
Labeler
bayer healthcare llc.
Dosage Form
KIT
Routes
Manufacturer
Identifiers & Regulatory
Product NDC
0280-0506
Product ID
0280-0506_45266d30-bb3b-21f8-e063-6294a90a29cf
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2017-05-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02800506
Hyphenated Format
0280-0506
Supplemental Identifiers
RxCUI
UPC
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
alka-seltzer plus severe cough mucus and congestion day and night (source: ndc)
Generic Name
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, guaifenesin (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg
- 10 mg
- 200 mg
- 5 mg
- 325 mg
- 6.25 mg
Packaging
- 1 KIT in 1 CARTON (0280-0506-20) * 2 BLISTER PACK in 1 CARTON / 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 2 BLISTER PACK in 1 CARTON / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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