REZAMID description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

REZAMID

Summers Laboratories Inc




FULL PRESCRIBING INFORMATION

Active ingredient

ACTIVE INGREDIENT

SULFUR 5%

RESORCINOL 2%

Purpose

PURPOSE

ACNE TREATMENT LOTION

Uses

USE

DRIES UP ACNE PIMPLES, HELPS PREVENT NEW PIMPLES

WARNINGS

  • FOR EXTERNAL USE ONLY

DO NOT USE

  • ON BROKEN SKIN
  • ON LARGE AREAS OF THE BODY

WHEN USING THIS PRODUCT

  • APPLY TO AFFECTED AREAS ONLY
  • DO NOT GET INTO EYES
  • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time

STOP USE AND ASK A DOCTOR IF

  • IF SKIN IRRITATION OCCURS OR GETS WORSE

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

Directions

  • shake very well before using
  • clean the skin thoroughly before applying this product
  • cover the entire affected area with a thin layer one to three times daily
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Inactive ingredients

water, SD-40 alcohol 28%, zinc oxide, talc, titanium dioxide, propylene glycol, attapulgite, lauramide DEA, iron oxides, sodium bisulfite, PEG-8 laurate, parachlorometaxylenol, hydroxyethylcellulose, sodium chloride, sodium polynapthalene sulfonate, EDTA, methyl paraben, xanthan gum, butylparaben, fragrance, simethicone.

REZAMID

REZAMID

SULFUR AND RESORCINOL LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11086-022
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SULFUR SULFUR 5 g
RESORCINOL RESORCINOL 2 1

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL
Zinc Oxide
talc
titanium dioxide
propylene glycol
ATTAPULGITE
LAURIC DIETHANOLAMIDE
ferric oxide red
SODIUM BISULFITE
PEG-8 LAURATE
Chloroxylenol
HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%)
SODIUM CHLORIDE
SODIUM NAPHTHALENESULFONATE
EDETIC ACID
METHYLPARABEN
XANTHAN GUM
BUTYLPARABEN
DIMETHICONE
SILICON

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11086-022-01 56.7 in 1 BOTTLE
2 NDC:11086-022-11 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partD part333D 2013-10-30


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.