Label: INTIMATE WIPE- benzocaine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 69681-434-04 - Packager: Veru Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 June 8, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
- Keep out of reach of children.
- Directions
- Inactive ingredients
- Principal Display Panel – Box Label
- Principal Display Panel – Packet Label
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INGREDIENTS AND APPEARANCE
INTIMATE WIPE
benzocaine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69681-434 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength benzocaine (UNII: U3RSY48JW5) (benzocaine - UNII:U3RSY48JW5) benzocaine 4 g in 100 mL Inactive Ingredients Ingredient Name Strength alcohol (UNII: 3K9958V90M) water (UNII: 059QF0KO0R) propylene glycol (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69681-434-04 4 in 1 BOX 06/08/2020 1 1.2 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part348 06/08/2020 Labeler - Veru Inc. (055300578) Registrant - Safetec of America, Inc. (874965262)