Label: INSECT BITE RELIEF- benzocaine solution
- NDC Code(s): 65734-300-00, 65734-300-36
- Packager: Swabplus Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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- Drug Fact
Benzocaine for Pain ReliefClose
temporary relief of pain and itching associated with insect bites, scrapes, minor cuts, minor burns, sunburn, or skin irritationClose
For external use only. do not bandage.
Do not use. in the eyes or apply over large areas of the body, particularly over raw surfaces or blistered area - if product gets into the eyes. flush throughly with water and obtain medical attention. longer than one week unless directed by doctor.
Stop use and ask a doctor if. condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days.Close
- Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.Close
♦ Do not use if label seal is broken prior to purchase. Keep swabs in original container when not in use.
♦ Hold the swab vertically, with the color band tip upwards. hold in the center of the stem with one hand and at the color band with the other.
♦ Bend the tip at the color band to one side until it snaps.
♦ Apply the product to the affected area.
♦ Discard swab after use.Close
For adult and children 2 and older. Apply directly onto affected area no more than 3 to 4 times daily.
Children under 2 years of age. Do not use, consult a doctor.Close
- Other information
Avoid storing at excessive heat.Close
- Inactive ingredients
Aloe Vera Gel. Ethoxydiglycol (diethylene glycol monoethyl ether), Glycerin, Menthol, PEG-8 (Polyethylene glycol 400), Propylene Glycol, TriclosanClose
- Package Display Panel
Image of insect bite carton label
- INGREDIENTS AND APPEARANCE
INSECT BITE RELIEF
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65734-300 Route of Administration TOPICAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5) Benzocaine 150 mg in 1 mL Inactive Ingredients Ingredient Name Strength Polyethylene Glycol 400 (UNII: B697894SGQ) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) Glycerin (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALOE VERA LEAF (UNII: ZY81Z83H0X) Triclosan (UNII: 4NM5039Y5X) Menthol (UNII: L7T10EIP3A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65734-300-36 36 in 1 PACKAGE 1 NDC:65734-300-00 0.15 mL in 1 APPLICATOR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part346 03/01/2003 Labeler - Swabplus Inc. (876441549) Registrant - Swabplus Inc. (876441549) Establishment Name Address ID/FEI Business Operations Swabplus Inc. 876441549 manufacture(65734-300) , relabel(65734-300) , repack(65734-300)