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NDC 24385-0251-10 Sinus Wash Saline Packets 700; 2300 mg/3000mg; mg/3000mg Details

Sinus Wash Saline Packets 700; 2300 mg/3000mg; mg/3000mg

Sinus Wash Saline Packets is a NASAL POWDER, FOR SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by AMERISOURCE BEGEN. The primary component is SODIUM BICARBONATE; SODIUM CHLORIDE.

Product Information

NDC	24385-0251
Product ID	24385-251_d52b1f0b-8f95-d347-e053-2a95a90a7d3b
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Sinus Wash Saline Packets
Proprietary Name Suffix	Good Neighbor Pharmacy
Non-Proprietary Name	SODIUM BICARBONATE, SODIUM CHLORIDE
Product Type	HUMAN OTC DRUG
Dosage Form	POWDER, FOR SOLUTION
Route	NASAL
Active Ingredient Strength	700; 2300
Active Ingredient Units	mg/3000mg; mg/3000mg
Substance Name	SODIUM BICARBONATE; SODIUM CHLORIDE
Labeler Name	AMERISOURCE BEGEN
Pharmaceutical Class	Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA],
DEA Schedule	n/a
Marketing Category	UNAPPROVED DRUG OTHER
Application Number	n/a
Listing Certified Through	2024-12-31

Package

Package Images

NDC 24385-0251-10 (24385025110)

Pricing Information	N/A
NDC Package Code	24385-251-10
Billing NDC	24385025110
Package	100 PACKET in 1 CARTON (24385-251-10) / 3000 mg in 1 PACKET (24385-251-01)
Marketing Start Date	2022-01-08
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL d52b1eff-5ec6-0de5-e053-2995a90ab20d Details

SPL UNCLASSIFIED SECTION

Active ingredients

(in each packet)

Sodium Bicarbonate USP (700 mg)

Sodium Chloride USP (2300 mg)

SPL UNCLASSIFIED SECTION

Purpose

Nasal Wash

SPL UNCLASSIFIED SECTION

Uses

Temporarily relieves symptoms associated with

sinusitis, cold, flu or allergies

-Sneezing

-Nasal stuffiness

-Runny nose

-Post nasal drip

Removes inhaled irritants (dust, pollen)

Removes nasal and sinus drainage

Helps reduce swelling of nasal membranes

Moisturizes dry nasal passages

SPL UNCLASSIFIED SECTION

Keep out of reach of children

SPL UNCLASSIFIED SECTION

Warnings

Stop use and ask a doctor if washing is uncomfortable or symptoms are not relieved.

Do not use unfiltered tap water. see instructions inside box for proper water sources

Do not use if nasal passages are completely blocked or if you have an ear infection or blocked ears

SPL UNCLASSIFIED SECTION

Directions

Adults and children 4 years and over: Use 1-2 packets per 8 fl oz (240 mL) up to every 2 hours as needed.

Children under 4 years: Consult a physician

See enclosed instruction sheet for complete directions and proper use.

SPL UNCLASSIFIED SECTION

Inactive ingredients

None

SPL UNCLASSIFIED SECTION

Other Information

-Inspect saline packets for integrity

-Do not use saline packets if open or torn

-Protect saline packets from excessive heat and moisture

-See saline packets or box for lot # and expiration date

SPL UNCLASSIFIED SECTION

Questions?

1-888-547-5492

SPL UNCLASSIFIED SECTION

-See instruction sheet for use

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SINUS WASH SALINE PACKETS GOOD NEIGHBOR PHARMACY

sodium bicarbonate, sodium chloride powder, for solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:24385-251
Route of Administration	NASAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37, BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	700 mg in 3000 mg
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	2300 mg in 3000 mg

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:24385-251-10	100 in 1 CARTON	01/08/2022
1	NDC:24385-251-01	3000 mg in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		01/08/2022

Labeler - AMERISOURCE BEGEN (007914906)

Revised: 1/2022

Document Id: d52b1f0b-8f95-d347-e053-2a95a90a7d3b

Set id: d52b1eff-5ec6-0de5-e053-2995a90ab20d

Version: 1

Effective Time: 20220109

Search by Drug Name or NDC

NDC 24385-0251-10 Sinus Wash Saline Packets 700; 2300 mg/3000mg; mg/3000mg Details

Sinus Wash Saline Packets 700; 2300 mg/3000mg; mg/3000mg

Product Information

Package

Package Images

NDC 24385-0251-10 (24385025110)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL d52b1eff-5ec6-0de5-e053-2995a90ab20d Details

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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