REZAMID

Dosage form: lotion
Ingredients: SULFUR 5g in 100mL, RESORCINOL 21 in 100mL
Labeler: Summers Laboratories Inc
NDC code: 11086-022

Medically reviewed by Drugs.com. Last updated on Nov 10, 2023.

ACTIVE INGREDIENTS

SULFUR 5%

RESORCINOL 2%

PURPOSE

ACNE TREATMENT LOTION

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
sulfur and resorcinol lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11086-022
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (SULFUR)	SULFUR	5 g in 100 mL
RESORCINOL (RESORCINOL)	RESORCINOL	2 in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER
ALCOHOL	28 mL in 100 mL
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
1	NDC:11086-022-01	56.7 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	10/30/2013

Labeler - Summers Laboratories Inc (002382612)

Establishment
Name	Address	ID/FEI	Operations
Summers Laboratories Inc		002382612	manufacture(11086-022), pack(11086-022)

Document Id: 2321978e-d5a8-4bf3-8520-5adf4f9086ce

Set id: d02ace0b-7244-45d4-987f-eb569303a426

Version: 6

Effective Time: 20181120

Summers Laboratories Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer