FDA.reportPublic FDA data

Saline

Manufacturer
Uriel Pharmacy Inc
Effective date
2010-02-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:02:11

Label at a glance#

ProductSaline
Active ingredientSODIUM CHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Uses: Use according to standard homeopathic indications.

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Directions: Take contents of 1 vial once daily.

OTC-Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Natrum muriaticum (Sea Salt) 1X HPUS.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Water.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

Do not use section

OTC - DO NOT USE SECTION

Warnings:  Do not use if allergic to any ingredient.

Ask doctor section

OTC - ASK DOCTOR SECTION

For serious conditions, consult a doctor before use.

Pregnancy or breast feeding section

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or nursing, consult a doctor before use.

Questions section

OTC - QUESTIONS SECTION

Questions? Uriel Pharmacy

866 642-2858  East Troy, WI 53120 

www.urielpharmacy.com

NDC 48951-9998-1

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Saline

Homeopathic Vials

net vol. 10 ml (1/3 fl. oz.)

saline vials labelsaline vials label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-9998-12020-01-31C16284748780-19d75b9d0-b56f-f424-e053-dadaa90a57ceSaline Vials - 10 ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9998-1Saline10 in 1 BOXSOLUTION/ DROPS101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9998SALINE (SODIUM CHLORIDE) SOLUTION/ DROPS [URIEL PHARMACY INC]1Legacy NDC, 1 package rows20100203_a7ffcc20-103e-11df-8a39-0800200c9a66.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X1
SODIUM CATIONACTIVE MOIETYLYR4M0NH371
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-999848951-9998-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XACTIB

Source Document#

Source XML

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
fa4e73f6-1039-11df-8a39-0800200c9a66a7ffcc20-103e-11df-8a39-0800200c9a662010-02-02Exact identifier
spl id: fa4e73f6-1039-11df-8a39-0800200c9a66
spl set id: a7ffcc20-103e-11df-8a39-0800200c9a66

Reported adverse events (FAERS/openFDA)#

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