Label: TIGER DELAYSPRAY- lidocaine spray
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Contains inactivated NDC Code(s)
NDC Code(s): 59240-005-06, 59240-005-08, 59240-005-12 - Packager: Magverz 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 August 11, 2016
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Purpose
- Keep out of Reach of Children
- Indication and Usage
- Inactive Ingredients
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Warning
Allergy alert: do not use this product if you or your partner are allergic (sensitive) to local Anesthetics.
Do not use - on broken or inflamed skin -if your partner is pregnant
Ask a doctor before use if you have, or ever had, liver or kidney problems
Ask a doctor or pharmacist before use if you are already taking prescribed drugs
when using this product
- do not get into eyes
- do not inhale
- do not exceed 24 sprays in 24 hours
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Dosage and Administration
-apply 3 or more sprays, not to exceed 10, to the head and shaft of the penis before intercourse, or as directed by a doctor
-wash product after intercourse
-correct quantity and time of application will be determined by individual requirements and you should always use the minimum effective quantity
- Product Label
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INGREDIENTS AND APPEARANCE
TIGER DELAYSPRAY
lidocaine sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59240-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 10 mg in 100 mL Inactive Ingredients Ingredient Name Strength ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) STEARIC ACID (UNII: 4ELV7Z65AP) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59240-005-06 6 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/03/2017 2 NDC:59240-005-08 8 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/03/2017 3 NDC:59240-005-12 12 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/03/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part346 01/03/2017 Labeler - Magverz INC (078712269) Registrant - Magverz INC (078712269)
