Label: HERPECIN PAIN RELIEF- allantoin, benzethonium chloride, lidocaine hcl gel
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Contains inactivated NDC Code(s)
NDC Code(s): 71687-4000-1 - Packager: Focus Consumer Healthcare, LLC
- 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 April 1, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DRUG FACTS
- ACTIVE INGREDIENT
- PURPOSE
- USES
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WARNINGS
DO NOT USE
Do not use over large areas of the body or on deep or puncture wounds, animal bites or serious burns
WHEN USING THIS PRODUCT
■ keep out of eyes. Rinse with water to remove.
■ apply only to the affected area. Avoid applying directly inside the mouth.
- DIRECTIONS
- OTHER INFORMATION
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INACTIVE INGREDIENT
aloe barbadensis leaf juice, bisabolol, disodium EDTA, ethylhexylglycerin, glycerin, hydrolyzed jojoba esters, hydroxyethylcellulose, lysine HCl, melissa officinalis extract, mentha piperita (peppermint) oil, mentha viridis (spearmint) leaf oil, potassium hydroxide, sclerotium gum, water, zingiber officinale (ginger) root extract
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
HERPECIN PAIN RELIEF
allantoin, benzethonium chloride, lidocaine hcl gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71687-4000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE ANHYDROUS (UNII: EC2CNF7XFP) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 4 g in 100 g ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 2 g in 100 g BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.2 g in 100 g Inactive Ingredients Ingredient Name Strength HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) LYSINE HYDROCHLORIDE, DL- (UNII: 81478P92RJ) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALOE VERA LEAF (UNII: ZY81Z83H0X) LEVOMENOL (UNII: 24WE03BX2T) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) GINGER (UNII: C5529G5JPQ) HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W) SPEARMINT OIL (UNII: C3M81465G5) MELISSA OFFICINALIS (UNII: YF70189L0N) MENTHA PIPERITA (UNII: 79M2M2UDA9) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) BETASIZOFIRAN (UNII: 2X51AD1X3T) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71687-4000-1 1 in 1 CARTON 06/11/2021 1 4 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 06/11/2021 Labeler - Focus Consumer Healthcare, LLC (080743737)