FDA.reportPublic FDA data

ORAL ASSIST

Manufacturer
Feelgood Health | W Last
Effective date
2010-06-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:02:18

Label at a glance#

ProductORAL ASSIST
Active ingredientSALICYLIC ACID, SILICON DIOXIDE, BELLADONNA LEAF, MERCURIUS SOLUBILIS, FERRUM PHOSPHORICUM, CALCIUM SULFIDE
Label structure10 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION

Relieves tooth discomfort

DOSAGE & ADMINISTRATION SECTION

Dosage: Mix 10 drops in ¼ cup water and sip slowly. Repeat 3-5 times daily as needed until symptoms subside. If preferred, drops may be taken directly into the mouth.

Children under 12: Reduce dosage to 5 drops, 3-5 times daily.

GENERAL PRECAUTIONS SECTION

Caution: Consult your doctor if symptoms persist or worsen.

Keep this and all medicines out of reach of children

OTC - ACTIVE INGREDIENT SECTION

Ingredients: Each dose contains equal parts of Acidum salicylicum 6C (HPUS), Silicea 6X (HPUS), Belladonna 30C (HPUS), Merc sol 12C (HPUS), Ferrum phos 6X (HPUS), Hepar sulph 12C (HPUS),

INACTIVE INGREDIENT SECTION

Citricidal Extract (inactive ingredient).

PREGNANCY SECTION

If pregnant or breastfeeding, ask a health professional before use.

USER SAFETY WARNINGS SECTION

Contains no animal products, gluten, artificial flavors, preservatives, colorants or alcohol. Suitable for vegetarians and safe for all ages

INFORMATION FOR PATIENTS SECTION

All Native Remedies health products are especially formulated by experts in the  field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness

The letters HPUS indicate that the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopoeia of the United States.

Distributed by

Native Remedies, LLC

6531 Park of Commerce

Blvd.  Suite C-160

Boca Raton, FL 33487

Phone: +1.877.289.1235

International: +1.253.620.4542

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle labelBottle label

INDICATIONS & USAGE SECTION

Indications:Homeopathic remedy for short-term relief of tooth discomfort and boils.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68647-172-102019-10-21C16284748780-1956f9ecf-ced3-621f-e053-dbdaa90a74adORAL ASSIST

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68647-172-10ORAL ASSIST100 mg in 1 BOTTLE, GLASSTINCTURE1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68647-172ORAL ASSIST TINCTURE [FEELGOOD HEALTH]2Legacy NDC, 1 package rows20100616_c606a9e9-39a0-482b-aaa7-c66b6a246eda.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BELLADONNA LEAFACTIVE INGREDIENT6GZW20TIOI2
CALCIUM SULFIDEACTIVE INGREDIENT1MBW07J51Q2
FERRUM PHOSPHORICUMACTIVE INGREDIENT91GQH8I5F72
MERCURIUS SOLUBILISACTIVE INGREDIENT324Y4038G22
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ2
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU42
BELLADONNA LEAFACTIVE MOIETY6GZW20TIOI2
CALCIUM CATIONACTIVE MOIETY2M83C4R6ZB2
FERRUM PHOSPHORICUMACTIVE MOIETY91GQH8I5F72
MERCURIUS SOLUBILISACTIVE MOIETY324Y4038G22
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ2
SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU42
GRAPEFRUIT SEEDINACTIVE INGREDIENT12F08874Y72
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68647-17268647-172-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
BELLADONNA LEAF6GZW20TIOIACTIB
MERCURIUS SOLUBILIS324Y4038G2ACTIB
FERRUM PHOSPHORICUM91GQH8I5F7ACTIB
CALCIUM SULFIDE1MBW07J51QACTIB
WATER059QF0KO0RIACT
GRAPEFRUIT SEED12F08874Y7IACT

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
eafeb411-a014-4dd0-98cd-866626884e53c606a9e9-39a0-482b-aaa7-c66b6a246eda2010-06-14Exact identifier
spl id: eafeb411-a014-4dd0-98cd-866626884e53
spl set id: c606a9e9-39a0-482b-aaa7-c66b6a246eda

Reported adverse events (FAERS/openFDA)#

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