Creomulsion

Manufacturer
Socius Care, LLC
Effective date
2026-02-17
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:46:03

Label at a glance#

ProductCreomulsion Cough Medicine Adult Formula
Active ingredientDEXTROMETHORPHAN HYDROBROMIDE
Label structure14 sections

Indications and uses

Temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold.

Dosage and administration

•Do not take more than 6 doses in any 24 period. Use enclosed dose cup. Adults and children 12 years and over 15mL (3 tsp) every 4 hours Children under 12 years do not use

Storage and handling

store at 20-25°C (68-77°F) packaged with tamper-evident seal under the cap contains no alcohol each 15 mL contains 5 mg sodium

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

In each (3 tsp) 15 ml Dextromethorphan HBr, USP 20 mg

Purpose

OTC - PURPOSE SECTION

Cough Suppressant

Uses

INDICATIONS & USAGE SECTION

  • Temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold.

Warnings

WARNINGS SECTION

Do not use if you are now taking prescription monoamine oxidase inhibitor (MAOI)

(certain drugs for depression, psychiatric; or emotional conditions, or Parkinson's disease),

or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or a pharmacist before taking this product.

Ask a doctor before use if you

OTC - ASK DOCTOR SECTION

  • have cough that occurs with too much phlegm (mucus)
  • have cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

•Do not take more than 6 doses in any 24 period. Use enclosed dose cup.

Adults and children 12 years and over15mL (3 tsp) every 4 hours
Children under 12 yearsdo not use

Other Information

STORAGE AND HANDLING SECTION

  • store at 20-25°C (68-77°F)
  • packaged with tamper-evident seal under the cap
  • contains no alcohol
  • each 15 mL contains 5 mg sodium

Inactive ingredients

INACTIVE INGREDIENT SECTION

beechwood creosote, caramel, citric acid, corn syrup, menthol, potassium sorbate, purified water, sodium benzoate, sucrose

Questions or Comments

OTC - QUESTIONS SECTION

Call 8am - 4pm Est. Mon - Fri. 1-404-566-8896

Money Back Guarantee

Guaranteed to give desired results or your money back.

Send carton top, reason for dissatisfaction, sales receipt, lot number, and your phone number to Socius Care, LLC

3939 Royal Dr. NW, Suite 230, Kennesaw, GA 30144

DESCRIPTION SECTION

How Creomulsion Cough Medicine Works?

The Creomulsion Cough Medicine contains a safe and effective cough suppressant which acts by temporarily calming the cough control center to relieve coughs. Its rich, traditional base coats and soothes raw, irritated membranes. It contains no dyes, no alcohol, and no artificial sweeteners.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Creomulsion Adult Back LabelCreomulsion Adult Back LabelCreomulsion Adult Front LabelCreomulsion Adult Front Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1246340Creomulsion 20 MG in 15 mL Oral SolutionPSN9
1246338dextromethorphan HBr 20 MG in 15 mL Oral SolutionPSN9
1246340dextromethorphan hydrobromide 1.33 MG/ML Oral Solution [Creomulsion]SBD9
1246338dextromethorphan hydrobromide 1.33 MG/ML Oral SolutionSCD9
1246340Creomulsion 1.33 MG/ML Oral SolutionSY9
1246340Creomulsion 20 MG per 15 ML SyrupSY9
1246338dextromethorphan hydrobromide 20 MG per 15 ML Oral SolutionSY9

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DEXTROMETHORPHAN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bf324df6-7127-7deb-def5-2681c136cd03Product name320250325
43a1ed49-eae2-4840-8075-cb4b33478540Product name120230425
ba088a92-ab5e-b2d4-e908-f5ea691b7587Product name720210201
76633df9-0d59-4b88-03ed-21dee1b966f8Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70893-0011-0CreomulsionCough Medicine Adult Formula1 in 1 CARTONSYRUP19
70893-0011-1CreomulsionCough Medicine Adult Formula118 mL in 1 BOTTLESYRUP1189

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70893-001170893-0011-1, 70893-0011-0

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82025-12-17monthly-update2026-06-03 17:46:09

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Creomulsion Cough Medicine Adult FormulaDEXTROMETHORPHAN HYDROBROMIDESocius Care, LLC39d07486-99b7-5c06-e054-00144ff8d46c2026-02-17WarningsExact identifier
ndc (package): 70893-0011-1
ndc (package): 70893-0011-0
ndc (product): 70893-0011
ndc11 (package): 70893001101
ndc11 (package): 70893001100
spl id: 4b0cae9f-cd7d-3372-e063-6294a90ad356
spl set id: 39d07486-99b7-5c06-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.