VTING- menthol liquid

United States - English - NLM (National Library of Medicine)

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Active ingredient:
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)
Available from:
VTING
Administration route:
TOPICAL
Prescription type:
OTC DRUG
Therapeutic indications:
Topical analgesic Temporary relieves minor aches and pains of muscle and joints associated with backache, arthritis, strains, bruises and sprains.
Authorization status:
OTC monograph not final
Authorization number:
81222-001-01, 81222-001-02

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VTING- menthol liquid

VTING

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they

comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

81222-001_VTING

Drug Facts

Active Ingredient

Menthol 0.9%

Purpos e

Topical analgesic

Us es

Temporary relieves minor aches and pains of muscle and joints associated with backache, arthritis,

strains, bruises and sprains.

Warnings

For external use only

When using this product

Avoid contact with eyes.

Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up

and occur again within a few days, discontinue use of this product and consult a physician.

Keep out of reach of children.

Directions

Adults and children 2 years of age and older: Apply to affected areas not more than 3 to 4 times daily.

Children under 2 years of age: consult a physician.

Inactive ingredients

Alcohol, Water, Dipropylene Glycol, Ceteareth-20, Camphor, Lavandula angustifolia (lavender) oil,

Caffeine, Carnitine, Piper methysticum root Extract, Centella Asiatica Extract, Aloe barbadensis leaf

juice, Gynostemma pentaphyllum leaf extract, FD&C BLUE NO. 1 (CI 42090), Linalool, Coumarin,

Geraniol, Benzyl benzoate

PRINCIPAL DISPLAY PANEL

VTING

menthol liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:8 1222-0 0 1

Route of Administration

TOPICAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

MENTHO L, UNSPECIFIED FO RM (UNII: L7T10 EIP3A) (MENTHOL, UNSPECIFIED FORM -

UNII:L7T10 EIP3A)

MENTHOL, UNSPECIFIED

FORM

0 .9 g

in 10 0 mL

Inactive Ingredients

Ingredient Name

Stre ng th

ALCO HO L (UNII: 3K9 9 58 V9 0 M)

WATER (UNII: 0 59 QF0 KO0 R)

DIPRO PYLENE GLYCO L (UNII: E10 7L8 5C40 )

PO LYO XYL 2 0 CETO STEARYL ETHER (UNII: YRC528 SWUY)

CAFFEINE (UNII: 3G6 A5W338 E)

CARNITINE (UNII: S7UI8 SM58 A)

MACRO PIPER METHYSTICUM RO O T (UNII: BOW48 C8 1XP)

VTING

CENTELLA ASIATICA WHO LE (UNII: 7M8 6 7G6 T1U)

ALO E VERA LEAF (UNII: ZY8 1Z8 3H0 X)

GYNO STEMMA PENTAPHYLLUM LEAF (UNII: 5DWS8 4R8 5M)

LAVENDER O IL (UNII: ZBP1YXW0 H8 )

FD&C BLUE NO . 1 (UNII: H3R47K3TBD)

LINALO O L, ( +/-) - (UNII: D8 1QY6 I8 8 E)

CO UMARIN (UNII: A4VZ22K1WT)

GERANIO L (UNII: L8 3710 8 USY)

BENZYL BENZO ATE (UNII: N8 6 3NB338 G)

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End

Date

1

NDC:8 1222-0 0 1-

1 in 1 CARTON

12/0 8 /20 20

1

NDC:8 1222-0 0 1-

50 0 mL in 1 BOTTLE, PUMP; Type 0 : No t a Co mbinatio n

Pro duc t

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

OTC mo no graph no t final

pa rt348

12/0 8 /20 20

Labeler -

VT ING (695126440)

Registrant -

VT ING (695126440)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Natural Ko rea Co ., Ltd.

6 8 8 729 438

ma nufa c ture (8 1222-0 0 1)

Revised: 12/2020

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