Label: INTIMALE BENZOCAINE DELAY GEL- benzocaine gel
- NDC Code(s): 81923-369-00
- Packager: SKINS SEXUAL HEALTH LIMITED
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2023
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- DRUG FACTS
- ACTIVE INGREDIENT:
- USES:
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WARNINGS:
• Premature ejaculation may be due to a condition requiring medical supervision. If this product, when used as directed, does not provide relief, discontinue use and consult a physician. If you or your partner develop a rash or irritation, such as burning or itching, discontinue use and consult a physician.
FOR EXTERNAL USE ONLY.• Avoid contact with eyes. - DIRECTIONS:
- Other Information:
- INACTIVE INGREDIENTS:
- QUESTIONS?
- Package Labeling:
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INGREDIENTS AND APPEARANCE
INTIMALE BENZOCAINE DELAY GEL
benzocaine gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81923-369 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) ARGININE (UNII: 94ZLA3W45F) ASIAN GINSENG (UNII: CUQ3A77YXI) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81923-369-00 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/03/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 10/03/2022 Labeler - SKINS SEXUAL HEALTH LIMITED (221947744)