Land: Bandaríkin
Tungumál: enska
Heimild: NLM (National Library of Medicine)
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN ZINC - UNII:89Y4M234ES)
Dynarex Corporation
BACITRACIN ZINC
BACITRACIN ZINC 500 [iU] in 1 g
TOPICAL
OTC DRUG
- Minor cuts - scrapes - burns - in case of deep or puncture wounds, animal bites and serious burns - if the condition persists or gets worse - if a rash or any other allergic reaction develops Indications and Usage - For first aid to help prevent infection in minor skin abrasions and rashes. Do not use: - in the eyes - over large area of the body - if you are allergic to any of the ingredients, due to the possibility of anaphylactic shock - longer than 1 week unless directed by a doctor
OTC monograph final
BACITRACIN ZINC - BACITRACIN ZINC OINTMENT DYNAREX CORPORATION _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._ ---------- BACITRACIN ZINC ACTIVE INGREDIENT PURPOSE Bacitracin Zinc 500 Units Antibactrerial US ES : First aid to help prevent infection in: Minor cuts scrapes burns ASK A DOCTOR BEFORE USE: in case of deep or puncture wounds, animal bites and serious burns if the condition persists or gets worse if a rash or any other allergic reaction develops OTHER INFORMATION store at controlled room temperature 15°-30° C (59°-86° F) Tamper Evident. Do not use if packet is torn, cut or opened. INACTIVE INGREDIENTS White Petrolatum Indications and Usage For first aid to help prevent infection in minor skin abrasions and rashes. DIRECTIONS : clean the affected area apply a small amount of this product (an amount equal to the surface area of the tip of the finger) on the area 1-3 times daily. may be covered with a sterile bandage KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, get medical help or contact a Poison Control Center right away. FOR EXTERNAL USE ONLY DO NOT USE: Do not use: in the eyes over large area of the body if you are allergic to any of the ingredients, due to the possibility of anaphylactic shock longer than 1 week unless directed by a doctor PRINCIPAL DISPLAY PANEL Principal Display Panel BACITRACIN ZINC bacitracin zinc ointment PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:6 7777-239 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH BACITRACIN ZINC (UNII: 8 9 Y4M234ES) (BACITRACIN ZINC - UNII:8 9 Y4M234ES) BACITRACIN ZINC 50 0 [iU] in 1 g INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH PETRO LATUM (UNII: 4T6 H12BN9 U) PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:6 7777-239 -0 1 12 in 1 CASE Dynarex Corporation 1 Lestu allt skjalið