Label: QUALITY CHOICE VAGINAL ANTI-ITCH MAXIMUM STRENGTH- benzocaine and resorcinol cream
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Contains inactivated NDC Code(s)
NDC Code(s): 63868-965-01 - Packager: Chain Drug Marketing Association (CDMA)
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated January 24, 2018
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients:
- Purpose
- Use:
- Warnings
- Directions:
- Other information
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Inactive ingredients
purified water, mineral oil, isopropyl palmitate, cetyl alcohol, PEG-100 stearate, glyceryl stearate, isopropyl myristate, lanolin, methyl-4 hydroxybenzoate, carbomer, fragrance, disodium EDTA, triethanolamine, propylene glycol, stearic acid corn oil, stearyl alcohol, vitamin A, E & D, aloe vera gel.
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Principal Display Panel - 1 oz. Carton Label
QC®
QUALITY
CHOICE
*Compare to active
ingredients in VAGISIL®
Maximum StrengthMaximum Strength
Vaginal Anti-Itch Cream
Medicated
20% Benzocaine | Resorcinol 3%
Long-Lasting Relief from:
Every Day Itching and Irritating Vaginal Conditions
Relieves Every Day Itch
QC®
QUALITY
CHOICE
Vaginal Anti-Itch Cream
Maximum Strength
1 OZ NET WT (28.4g)
- Principal Display Panel - 1 oz. Tube Label
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INGREDIENTS AND APPEARANCE
QUALITY CHOICE VAGINAL ANTI-ITCH MAXIMUM STRENGTH
benzocaine and resorcinol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-965 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 200 mg in 1 g RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK) RESORCINOL 30 mg in 1 g Inactive Ingredients Ingredient Name Strength Aloe Vera Leaf (UNII: ZY81Z83H0X) Carbomer Copolymer Type B (Allyl Pentaerythritol Crosslinked) (UNII: 809Y72KV36) Cetyl Alcohol (UNII: 936JST6JCN) Edetate Disodium (UNII: 7FLD91C86K) Glyceryl Monostearate (UNII: 230OU9XXE4) Isopropyl Myristate (UNII: 0RE8K4LNJS) Isopropyl Palmitate (UNII: 8CRQ2TH63M) Lanolin (UNII: 7EV65EAW6H) Potassium Methylparaben (UNII: M64U971IB0) Mineral Oil (UNII: T5L8T28FGP) PEG-100 Stearate (UNII: YD01N1999R) Propylene Glycol (UNII: 6DC9Q167V3) Water (UNII: 059QF0KO0R) Stearic Acid (UNII: 4ELV7Z65AP) Stearyl Alcohol (UNII: 2KR89I4H1Y) Trolamine (UNII: 9O3K93S3TK) Vitamin A (UNII: 81G40H8B0T) Vitamin D (UNII: 9VU1KI44GP) .Alpha.-Tocopherol (UNII: H4N855PNZ1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-965-01 1 in 1 CARTON 04/28/2014 1 28 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 04/28/2014 Labeler - Chain Drug Marketing Association (CDMA) (011920774) Establishment Name Address ID/FEI Business Operations Natural Essentials 947484713 MANUFACTURE(63868-965)