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NDC 11673-0142-64 Up and up vagicaine 20; 3 g/100g; g/100g Details

Up and up vagicaine 20; 3 g/100g; g/100g

Up and up vagicaine is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Target Corporation. The primary component is BENZOCAINE; RESORCINOL.

Product Information

NDC	11673-0142
Product ID	11673-142_f7eabecd-9065-4bba-b2b3-06ad6050cbc8
Associated GPIs	55400002103740
GCN Sequence Number	050344
GCN Sequence Number Description	benzocaine/resorcin/aloe/E,A,D CREAM (G) 20 %-3 % TOPICAL
HIC3	Q5H
HIC3 Description	TOPICAL LOCAL ANESTHETICS
GCN	17355
HICL Sequence Number	035150
HICL Sequence Number Description	BENZOCAINE/RESORCINOL/ALOE VERA/VIT E ACET/VITAMINS A AND D
Brand/Generic	Generic
Proprietary Name	Up and up vagicaine
Proprietary Name Suffix	n/a
Non-Proprietary Name	Benzocaine, Resorcinol
Product Type	HUMAN OTC DRUG
Dosage Form	CREAM
Route	TOPICAL
Active Ingredient Strength	20; 3
Active Ingredient Units	g/100g; g/100g
Substance Name	BENZOCAINE; RESORCINOL
Labeler Name	Target Corporation
Pharmaceutical Class	Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part348
Listing Certified Through	2024-12-31

Package

Package Images

NDC 11673-0142-64 (11673014264)

Pricing Information	N/A
NDC Package Code	11673-142-64
Billing NDC	11673014264
Package	1 TUBE in 1 CARTON (11673-142-64) / 28 g in 1 TUBE
Marketing Start Date	2009-08-25
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL ea8b802b-7d79-43e2-a969-03c881d1a080 Details

Active ingredients

Benzocaine 20%

Resorcinol 3%

Purpose

External analgesic

Use

temporarily relieves itching

Warnings

For external use only

When using this product

avoid contact with the 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

Do not apply

over large areas of the body

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

adults and children 12 years and older	apply a fingertip amount (approximately 1-inch strip) to the affected area not more than 3 to 4 times daily. Clean nozzle of tube by wiping thoroughly before replacing cap. Keep cap tightly closed between uses.
children under 12 years	ask a doctor

Other information

store at 20-25°C (68-77°F)

Inactive ingredients

aloe barbadensis leaf juice, carbomer homopolymer type C, cetyl alcohol, cholecalciferol, corn (zea mays) oil, fragrance, glyceryl monostearate, isopropyl myristate, isopropyl palmitate, isopropyl stearate, lanolin alcohol, methylparaben, mineral oil, PEG-100 stearate, propylene glycol, purified water, retinyl palmitate, sodium sulfite anhydrous, tocopheryl acetate, trisodium HEDTA, trolamine

Questions?

Call 1-888-547-7400

Principal Display Panel

maximum strength

vagicaine

anti-itch cream

benzocaine 20% / resorcinol 3%

Compare to active ingredients in Vagisil® Maximum Strength

pain relieving cream

instant long-lasting relief from intense itch associated with: antibiotics, discharge, imbalance in pH, irritating vaginal conditions

NET WT 1 OZ (28 g)

INGREDIENTS AND APPEARANCE

UP AND UP VAGICAINE

benzocaine, resorcinol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11673-142
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	20 g in 100 g
RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK)	RESORCINOL	3 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
CETYL ALCOHOL (UNII: 936JST6JCN)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
CORN OIL (UNII: 8470G57WFM)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
ISOPROPYL STEARATE (UNII: 43253ZW1MZ)
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
METHYLPARABEN (UNII: A2I8C7HI9T)
MINERAL OIL (UNII: T5L8T28FGP)
PEG-100 STEARATE (UNII: YD01N1999R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
SODIUM SULFITE (UNII: VTK01UQK3G)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TRISODIUM HEDTA (UNII: K3E0U7O8KI)
TROLAMINE (UNII: 9O3K93S3TK)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:11673-142-64	1 in 1 CARTON	08/25/2009
1		28 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	08/25/2009

Labeler - Target Corporation (006961700)

Revised: 3/2019

Document Id: f7eabecd-9065-4bba-b2b3-06ad6050cbc8

Set id: ea8b802b-7d79-43e2-a969-03c881d1a080

Version: 5

Effective Time: 20190322