Label: HEMRID ANORECTAL CREAM- lidocaine cream
- NDC Code(s): 82620-001-01
- Packager: KKA & Associates LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2023
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- Official Label (Printer Friendly)
- INACTIVE INGREDIENT
- ACTIVE INGREDIENT
- PURPOSE
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DOSAGE & ADMINISTRATION
When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly, gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.
apply externally to the affected area up to 6 times a day.
Children under 12 years of age: consult a doctor.
To use with finger cot. Roll one finger cot over finger. Gently squeeze cream onto finger
Smooth a layer of the cream over the affected area. - KEEP OUT OF REACH OF CHILDREN
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WARNINGS
FOR EXTERNAL USE ONLY
When using this product
use only as directed.
Avoid contact with eyes.
do not exceed recommended dosage unless directed by a doctor.
do not out this product into the rectum by using fingers or any mechanical device or applicator.
Stop use and ask a doctor if
rectal bleeding occurs.
condition worsens or does not improve within 7 days.
symptoms clear up and occur again within a few days.
an allergic reaction develops to ingredients in this product.
symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase.
If pregnant or breast-feeding, ask a health professional before use. - INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HEMRID ANORECTAL CREAM
lidocaine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82620-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TROLAMINE (UNII: 9O3K93S3TK) .ALPHA.-TOCOPHEROL CALCIUM SUCCINATE, DL- (UNII: H5A1374A6R) CHOLESTEROL (UNII: 97C5T2UQ7J) WATER (UNII: 059QF0KO0R) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) CARBOMER 940 (UNII: 4Q93RCW27E) BENZYL ALCOHOL (UNII: LKG8494WBH) HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N) POLYSORBATE 80 (UNII: 6OZP39ZG8H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82620-001-01 1 in 1 CARTON 04/04/2022 1 28.3 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 04/04/2022 Labeler - KKA & Associates LLC (050979549)
