Land: USA
Språk: engelsk
Kilde: NLM (National Library of Medicine)
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)
Dynarex Corporation
TOPICAL
OTC DRUG
uses for temporary relief of pain and itching associated with insect bites and stings for temporary relief of pain and itching
unapproved drug other
MEDICAINE STING AND BITE- BENZOCAINE SWAB DYNAREX CORPORATION _Disclaimer: This drug has not been found by FDA to be safe and effective, and this_ _labeling has not been approved by FDA. For further information about unapproved_ _drugs, click here._ ---------- 1407 MEDICAINE INSECT BITE (AMPULE) 67777-405-01 active ingredient each swab has benzocaine usp, l menthol uses for temporary relief of pain and itching associated with insect bites and stings keep out of reach of children. not for use with children less than 2 years old without medical advice. if swallowed, get medical help immediately or contact a poison control center right away revers cardboard sleeve then crush at dot between thumb and forefinger. once solution has saturated tip, apply topically to the sting or bit. may be used on affected area(s) up to 4 times per day store at room temperature away from light purified water usp for temporary relief of pain and itching for external use only medicaine sting and bit ampules latex free MEDICAINE STING AND BITE benzocaine swab Dynarex Corporation PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:67777-405 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZ OCAINE 0.12 g in 0.6 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH MENTHOL (UNII: L7T10EIP3A) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:67777-405- 02 10 in 1 BOX 02/14/1976 1 NDC:67777-405- 01 6 mL in 1 AMPULE; Type 0: Not a Combination Product MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE unapproved drug other 02/14/1976 LABELER - Dynarex Corporation (008124539) REGISTRANT - Dynarex Corporation (008124529) Revised: 11/2022 read_full_document