robitussin day and night cough relief dm max

Generic: dextromethorphan hydrobromide, guaifenesin, doxylamine succinate

Labeler: haleon us holdings llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name robitussin day and night cough relief dm max
Generic Name dextromethorphan hydrobromide, guaifenesin, doxylamine succinate
Labeler haleon us holdings llc
Dosage Form KIT
Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0031-2834
Product ID 0031-2834_42637c25-c581-e5d5-e063-6394a90af1b5
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00312834
Hyphenated Format 0031-2834

Supplemental Identifiers

RxCUI
1020138 1115329 2056073

Packaging Origin

Original Packager
true

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 robitussin day and night cough relief dm max (source: ndc)
Generic Name dextromethorphan hydrobromide, guaifenesin, doxylamine succinate (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 20 ml
  • 20 mg
  • 400 mg
  • 30 mg
  • 12.5 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (0031-2834-01) * 1 BOTTLE in 1 CARTON (0031-8739-18) / 237 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0031-8718-18) / 237 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0031-8739-12) / 118 mL in 1 BOTTLE
source: ndc

Packages (1)

0031-2834-01 1 KIT in 1 CARTON (0031-2834-01) * 1 BOTTLE in 1 CARTON (0031-8739-18) / 237 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0031-8718-18) / 237 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0031-8739-12) / 118 mL in 1 BOTTLE

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Robitussin Day and Night Cough Relief DM Max ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "42637c25-c581-e5d5-e063-6394a90af1b5", "openfda": {"rxcui": ["1020138", "1115329", "2056073"], "spl_set_id": ["b3d02c91-8f79-4eb4-a378-1072474c572c"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0031-2834-01)  *  1 BOTTLE in 1 CARTON (0031-8739-18)  / 237 mL in 1 BOTTLE *  1 BOTTLE in 1 CARTON (0031-8718-18)  / 237 mL in 1 BOTTLE *  1 BOTTLE in 1 CARTON (0031-8739-12)  / 118 mL in 1 BOTTLE", "package_ndc": "0031-2834-01", "marketing_start_date": "20210301"}], "brand_name": "Robitussin Day and Night Cough Relief DM Max", "product_id": "0031-2834_42637c25-c581-e5d5-e063-6394a90af1b5", "dosage_form": "KIT", "product_ndc": "0031-2834", "generic_name": "dextromethorphan hydrobromide, guaifenesin, doxylamine succinate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Robitussin", "brand_name_suffix": "Day and Night Cough Relief DM Max", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}