VAGI CARE- benzocaine, benzalkonium chloride cream

Vagi care by

Drug Labeling and Warnings

Vagi care by is a Otc medication manufactured, distributed, or labeled by Personal Care Products, anicare pharmaceuticals pvt.ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Vagi Care

For external use only.

Avoid contact with eyes. In case of eye contact, flush with plenty of water. If irritation persist, seek medical advice.

Stop use and ask a doctor if conditin worsens, or if symptoms persist for more than 7 days or clear up and reoccur within a few days.

Do not apply over large areas of skin.

ACTIVE INGREDIENT

Active Ingredient

Benzocaine 5.0%

Benzalkonium Chloride 0.13%

WARNINGS

warnings

For external use only.

Avoid contact with eyes. In case of eye contact flush with plenty of water. If irritation persist, seek medical advice.

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

Do not apply over large areas of skin.

DOSAGE & ADMINISTRATION

Directions adults and children 2 years and older-Apply fingertip amount (approximately 1-inch strip) to affected area not more than 3 to 4 times daily

children under 2 years-consult a doctor

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

INDICATIONS & USAGE

Uses temporarily relieves itching

PURPOSE

Purpose External Analgesic

INACTIVE INGREDIENT

Aloe Barbadensis (aloe vera) gel, cetryl alcohol, diazolidinyl urea, dimethicone, glycol stearate, hydroxypropyl bisstearyldimonium chloride, methyl paraben, mineral oil, PEG 100 stearate, PEG 400, propyl paraben, prified water, tocopheryl acetate (vitamin e)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VAGI CARE 
benzocaine, benzalkonium chloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29500-2264
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	1.05 g  in 21 g
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.003 g  in 21 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCOL STEARATE (UNII: 0324G66D0E)
HYDROXYPROPYL BISSTEARYLDIMONIUM CHLORIDE (UNII: OVB1E9X12I)
METHYLPARABEN (UNII: A2I8C7HI9T)
MINERAL OIL (UNII: T5L8T28FGP)
PEG-100 STEARATE (UNII: YD01N1999R)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29500-2264-1	21 g in 1 TUBE; Type 0: Not a Combination Product	03/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	01/01/2013

Labeler - Personal Care Products (966155082)