Label: OFF BITE AND ITCH RELIEF FIRST AID ANTISEPTIC- benzocaine, phenol, camphor solution
- NDC Code(s): 59397-3310-1
- Packager: S. C. Johnson & Son, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 7, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
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Warnings
For external use only.
When using this product
- Do not get in eyes
- Do not apply over large areas of the body
- In case of deep or puncture wounds, animal bites, or serious burns consult a doctor.
- Do not bandage.
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Directions
- Clean the affected area. Apply a small amount of this product on the affected area while massaging with sponge tip applicator. If itching persists, apply again in 10-15 minutes.
- For ticks and bees, remove tick or stinger before treatment.
- Adults and children 2 years of age and older: Apply to affected area not more than 1-3 times daily. Children under 2 years of age: Consult a doctor.
- Inactive Ingredients
- Questions or Comments?
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL - 15 mL Bottle Label
SCJohnson
A Family CompanyForgot
Your OFF!®
Repellent?
Get Quick
Relief from
Bites & Itching.OFF!®
familycare
BITE AND ITCH RELIEFFIRST AID
ANTISEPTICTOUCH FREE NO MESS
APPLICATIONSOOTHES BITES FROM
MOSQUITOES AND
OTHER INSECTSRELIEVES ITCH FROM
POISON IVY,
POISON OAK, AND
POISON SUMACANTISEPTIC
RELIEVES ITCH
SPONGE TIP
APPLICATORNET 0.5 FL. OZ. (15 mL)
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INGREDIENTS AND APPEARANCE
OFF BITE AND ITCH RELIEF FIRST AID ANTISEPTIC
benzocaine, phenol, camphor solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59397-3310 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 5 mg in 100 mL PHENOL (UNII: 339NCG44TV) (PHENOL - UNII:339NCG44TV) PHENOL 1.35 mg in 100 mL CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL) 3 mg in 100 mL Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59397-3310-1 1 in 1 CARTON 11/01/2013 1 14.79 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M017 11/01/2013 Labeler - S. C. Johnson & Son, Inc. (006091417) Registrant - Wisconsin Pharmacal Company (800873986) Establishment Name Address ID/FEI Business Operations Wisconsin Pharmacal Company 800873986 manufacture(59397-3310)