ORAL ASSIST- oral assist tincture
W Last CC

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

----------

ORAL ASSIST

Relieves tooth discomfort

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.

Caution: Consult your doctor if symptoms persist or worsen.

Keep this and all medicines out of reach of children

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),

Citricidal Extract (inactive ingredient).

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

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

All Native Remedies health products are especially formulated by experts in thefield 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

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

Bottle label

ORAL ASSIST
oral assist tincture

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50048-015
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	6 [hp_C] in 33.33 mg
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	6 [hp_X] in 33.33 mg
BELLADONNA LEAF (UNII: 6GZW20TIOI) (BELLADONNA LEAF - UNII:6GZW20TIOI)	BELLADONNA LEAF	30 [hp_C] in 33.33 mg
MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2)	MERCURIUS SOLUBILIS	12 [hp_C] in 33.33 mg
FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7)	FERROSOFERRIC PHOSPHATE	6 [hp_X] in 33.33 mg
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q)	CALCIUM SULFIDE	12 [hp_C] in 33.33 mg

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CITRUS PARADISI SEED (UNII: 12F08874Y7)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50048-015-50	100 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	01/01/2010	01/09/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		01/01/2010	01/09/2019

Labeler - W Last CC (567284153)

Registrant - W Last CC (567284153)

Name	Address	ID/FEI	Business Operations
Establishment
W Last CC		567284153	manufacture(50048-015)

Revised: 1/2019

Document Id: 89edd6aa-43db-4f46-aa63-9e6e3a2ba910

Set id: 98a7076f-38dd-42b9-9191-a311dd515e82

Version: 3

Effective Time: 20190109

W Last CC