Label: HEMOTREAT- white petrolatum, lanolin, hard fat, camphor cream
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Contains inactivated NDC Code(s)
NDC Code(s): 69758-322-55, 69758-322-71 - Packager: Global Treat srl
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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.
Drug Label Information
Updated May 27, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Purposes
- Uses
- Warnings
- DO NOT USE
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Stop use and ask a doctor if:
- bleeding occurs
- condition worsens or does not improve within seven days
- signs of a local infection appear
- Certain person can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside of if redness, irritation, swelling, pain, and or other symptoms develop or increase, discontinue use and consult a doctor.
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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Directions
Adults
- when practical, cleanse the affected area with mild soap and warm water
- gently dry by patting or blotting with toilet tissue or a soft cloth before application of ointment
- with the help of the index finger, apply a thin layer of ointment
- apply 2 times a day, morning and evening, for 5-7 days. Spread on to the affected area, generally on the exterior of the anus and in the vicinity of the anal orifice
Children under 12 years
- consult a doctor
- Other Information
- Inactive Ingredients
- QUESTIONS
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
HEMOTREAT
white petrolatum, lanolin, hard fat, camphor creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69758-322 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 0.213 g in 1 g LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H) LANOLIN 0.212 g in 1 g FAT, HARD (UNII: 8334LX7S21) (FAT, HARD - UNII:8334LX7S21) FAT, HARD 0.426 g in 1 g CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 0.025 g in 1 g Inactive Ingredients Ingredient Name Strength BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U) CALCIUM CARBONATE (UNII: H0G9379FGK) ALCOHOL (UNII: 3K9958V90M) ETHYLPARABEN (UNII: 14255EXE39) EUCALYPTUS OIL (UNII: 2R04ONI662) METHYLPARABEN (UNII: A2I8C7HI9T) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69758-322-55 50 g in 1 JAR; Type 0: Not a Combination Product 05/15/2015 02/15/2018 2 NDC:69758-322-71 1 in 1 CARTON 06/01/2016 2 28.3 g in 1 TUBE, 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 final part346 05/15/2015 Labeler - Global Treat srl (505948710)
