Label: BITE AND STING RELIEF WIPE- alcohol 50% lidocaine hcl 2% cloth
- 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.
Updated July 5, 2019
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- Active Ingredients
For external use only.
Flammable, keep away from fire or flame.
Do not use
- in the eyes over large areas of the body or bandage.
- in large quantities particularly over raw surfaces or blistered areas.
- Keep out of reach of children
- Inactive ingredients
INGREDIENTS AND APPEARANCE
BITE AND STING RELIEF WIPE
alcohol 50% lidocaine hcl 2% cloth
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-190 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 50 mL in 100 mL LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 2 g in 100 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) MENTHOL (UNII: L7T10EIP3A) WATER (UNII: 059QF0KO0R) Product Characteristics Color white Score Shape RECTANGLE Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-190-10 30 in 1 BOX 06/01/2019 1 3 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 not final part348 06/01/2019 Labeler - CVS (062312574) Establishment Name Address ID/FEI Business Operations Diamond Wipes International, Inc. 161104729 manufacture(69842-190)