TING CREAM- undecylenic acid, triclosan cream

TING by

Drug Labeling and Warnings

TING by is a Otc medication manufactured, distributed, or labeled by ALL NATURAL DYNAMICS, Farmaqro, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (Each 100 g contains:)

Purpose

Undecylenic Acid Antifungal

Triclosan Antibacterial

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

TING® CREAM kills fungi that cause athlete's foot and effectively eliminates odor-causing bacteria (deodorant).

TING® CREAM has double action: anti-fungal (fungicide) and bacteria (antiseptic).

TING® CREAM quickly eliminates sweating, itching, odor, burning and cracking.

Warnings

Do not use in patients allergic to the formula, or near the eyes and/or mucous membranes, do not administer to children under 2 years of age.

Side effects: There may appear slight manifestations of the local irritation.

If symptoms persist consult your physician.

Directions

Before applying TING ® CREAM wash your feet with soap and water and dry thoroughly.

Apply TING ® CREAM gently rub it on the affected area in the morning and at bedtime.

It is very important to pay special attention to spaces between the toes.

Once you have cleared the lesions and symptoms treatment should be continued 15 days.

Inactive ingredient

None

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TING  CREAM
undecylenic acid, triclosan cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51769-003
Route of Administration	Cutaneous

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Undecylenic acid (UNII: K3D86KJ24N) (UNDECYLENIC ACID - UNII:K3D86KJ24N)	Undecylenic acid	3.780 g  in 100 g
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	.100 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
Petrolatum (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51769-003-48	48 g in 1 TUBE
2	NDC: 51769-003-72	72 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	03/15/2013

Labeler - ALL NATURAL DYNAMICS (962732892)

Establishment
Name	Address	ID/FEI	Business Operations
Farmaqro, S.A. de C.V.		588161468	manufacture(51769-003)