Search by Drug Name or NDC

NDC 41163-0630-26 equaline anti nausea 1.87; 1.87; 21.5 g/5mL; g/5mL; mg/5mL Details

equaline anti nausea 1.87; 1.87; 21.5 g/5mL; g/5mL; mg/5mL

equaline anti nausea is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by Supervalu Inc. The primary component is DEXTROSE; FRUCTOSE; PHOSPHORIC ACID.

Product Information

NDC	41163-0630
Product ID	41163-630_4e1bd9fe-3025-4125-9e3e-230d5b87c337
Associated GPIs
GCN Sequence Number	004698
GCN Sequence Number Description	phosphorated carbo(dext-fruct) SOLUTION ORAL
HIC3	H6J
HIC3 Description	ANTIEMETIC/ANTIVERTIGO AGENTS
GCN	73710
HICL Sequence Number	015060
HICL Sequence Number Description	PHOSPHORATED CARBOHYDRATE (DEXTROSE AND FRUCTOSE)
Brand/Generic	Generic
Proprietary Name	equaline anti nausea
Proprietary Name Suffix	n/a
Non-Proprietary Name	Dextrose (glucose), Levulose (fructose), Phosphoric Acid
Product Type	HUMAN OTC DRUG
Dosage Form	SOLUTION
Route	ORAL
Active Ingredient Strength	1.87; 1.87; 21.5
Active Ingredient Units	g/5mL; g/5mL; mg/5mL
Substance Name	DEXTROSE; FRUCTOSE; PHOSPHORIC ACID
Labeler Name	Supervalu Inc
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	UNAPPROVED DRUG OTHER
Application Number	n/a
Listing Certified Through	2023-12-31

Package

Package Images

NDC 41163-0630-26 (41163063026)

Pricing Information	N/A
NDC Package Code	41163-630-26
Billing NDC	41163063026
Package	1 BOTTLE in 1 CARTON (41163-630-26) / 118 mL in 1 BOTTLE
Marketing Start Date	2004-09-28
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL f3b7efe0-8d3c-4fc2-b878-c20b962e6266 Details

Active ingredients (per 5 mL)

Dextrose (glucose) 1.87g

Levulose (fructose) 1.87g

Phosphoric acid 21.5mg

Purpose

Upset stomach reliever

Uses

•: for relief of upset stomach associated with nausea

Warnings

•: this product contains fructose and should not be taken by persons with hereditary fructose intolerance (HFI)

Do not use

if you have

•: allergic reactions to any of the ingredients in this product

Ask a doctor before use if you have

•: diabetes

Stop use and ask a doctor if

•: symptoms persist, return or get worse

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

•: for maximum effectiveness, never dilute or drink fluids of any kind immediately before or after taking this product
•: repeat dose every 15 minutes or until distress subsides
•: do not take more than 5 doses in 1 hour without consulting a doctor
•: measure only with dosing cup provided. Dosing cup to be used with this product only. Do not use with other products.
•: mL = milliliters

age	dose
adults and children 12 years of age and over	15 mL or 30 mL
children 2 to under 12 years of age	5 mL or 10 mL

Other information

•: store at 20-25°C (68-77°F) away from heat and direct light; keep from freezing.
•: do not use if printed neckband is broken or missing

Inactive ingredients

FD&C red no. 40 aluminum lake, flavor, glycerin, methylparaben, purified water

Questions or comments?

1-877-932-7948

Package/Label Principal Display Panel

compare to Emetrol® active ingredients

anti-nausea liquid

for children and adults

safe for children with flu or fever

relief for nausea due to upset stomach

cherry flavor

NO ANTIHISTAMINES

NO ASPIRIN

NO ALCOHOL

NO CAFFEINE

4 FL OZ (118mL)

INGREDIENTS AND APPEARANCE

EQUALINE ANTI NAUSEA

dextrose (glucose), levulose (fructose), phosphoric acid solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:41163-630
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
DEXTROSE (UNII: IY9XDZ35W2) (DEXTROSE - UNII:IY9XDZ35W2)	DEXTROSE	1.87 g in 5 mL
FRUCTOSE (UNII: 6YSS42VSEV) (FRUCTOSE - UNII:6YSS42VSEV)	FRUCTOSE	1.87 g in 5 mL
PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN)	PHOSPHORIC ACID	21.5 mg in 5 mL

Ingredient Name	Strength
Inactive Ingredients
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	RED (clear)	Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:41163-630-26	1 in 1 CARTON	09/28/2004
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
Unapproved drug other		09/28/2004

Labeler - Supervalu Inc (006961411)

Revised: 10/2018

Document Id: 4e1bd9fe-3025-4125-9e3e-230d5b87c337

Set id: f3b7efe0-8d3c-4fc2-b878-c20b962e6266

Version: 4

Effective Time: 20181011