Clindamycin Phosphate CLINDAMYCIN PHOSPHATE CHARTWELL RX, LLC FDA Approved Clindamycin Phosphate Topical Solution, USP contains Clindamycin Phosphate, USP, at a concentration equivalent to 10 mg clindamycin per milliliter. Clindamycin phosphate is a water soluble ester of the semi-synthetic antibiotic produced by a 7(S)-chloro-substitution of the 7(R)-hydroxyl group of the parent antibiotic lincomycin. The solution contains isopropyl alcohol 50% v/v, propylene glycol, sodium hydroxide, and purified water. The structural formula is represented below: The chemical name for clindamycin phosphate is Methyl-7-chloro-6,7,8-trideoxy-6-(1-methyl- trans -4-propyl-L-2-pyrrolidinecarboxamido)-1-thio-L- threo -α-D- galacto -octopyranoside 2-(dihydrogen phosphate). "Image Description"
FunFoxMeds bottle
Route
TOPICAL
Applications
ANDA209846

Drug Facts

Composition & Profile

Strengths
1 % 10 mg 30 ml 60 ml
Quantities
30 ml 60 ml
Treats Conditions
Indications And Usage Clindamycin Phosphate Topical Solution 1 Is Indicated In The Treatment Of Acne Vulgaris In View Of The Potential For Diarrhea Bloody Diarrhea And Pseudomembranous Colitis The Physician Should Consider Whether Other Agents Are More Appropriate See Contraindications Warnings And Adverse Reactions
Pill Appearance
Color: white

Identifiers & Packaging

Container Type BOTTLE
UPC
0362135478605
UNII
EH6D7113I8
Packaging

HOW SUPPLIED Clindamycin Phosphate Topical Solution, USP, 1% is clear, colorless solution free of foreign matter and crystallized particles containing clindamycin phosphate equivalent to 10 mg clindamycin per milliliter is available in the following size: 30 mL applicator bottle - NDC – 62135-478-30 60 mL applicator bottle - NDC – 62135-478-60 Store at controlled room temperature 20°C to 25°C (68°F to 77°F) [see USP]. Protect from freezing. Rx only To report SUSPECTED ADVERSE REACTIONS, contact FDA at 1-800-FDA-1088 or www.fda.gov/medwatch or Chartwell RX, LLC. at 1-845-232-1683. Manufactured for: Chartwell RX, LLC. Congers, NY 10920 L72665 Rev. 08/2025; PRINCIPAL DISPLAY PANEL Clindamycin Phosphate Topical Solution, USP 1% NDC - 62135-478-60 - 60 mL Bottle Label "Image Description"

Package Descriptions
  • HOW SUPPLIED Clindamycin Phosphate Topical Solution, USP, 1% is clear, colorless solution free of foreign matter and crystallized particles containing clindamycin phosphate equivalent to 10 mg clindamycin per milliliter is available in the following size: 30 mL applicator bottle - NDC – 62135-478-30 60 mL applicator bottle - NDC – 62135-478-60 Store at controlled room temperature 20°C to 25°C (68°F to 77°F) [see USP]. Protect from freezing. Rx only To report SUSPECTED ADVERSE REACTIONS, contact FDA at 1-800-FDA-1088 or www.fda.gov/medwatch or Chartwell RX, LLC. at 1-845-232-1683. Manufactured for: Chartwell RX, LLC. Congers, NY 10920 L72665 Rev. 08/2025
  • PRINCIPAL DISPLAY PANEL Clindamycin Phosphate Topical Solution, USP 1% NDC - 62135-478-60 - 60 mL Bottle Label "Image Description"

Overview

Clindamycin Phosphate Topical Solution, USP contains Clindamycin Phosphate, USP, at a concentration equivalent to 10 mg clindamycin per milliliter. Clindamycin phosphate is a water soluble ester of the semi-synthetic antibiotic produced by a 7(S)-chloro-substitution of the 7(R)-hydroxyl group of the parent antibiotic lincomycin. The solution contains isopropyl alcohol 50% v/v, propylene glycol, sodium hydroxide, and purified water. The structural formula is represented below: The chemical name for clindamycin phosphate is Methyl-7-chloro-6,7,8-trideoxy-6-(1-methyl- trans -4-propyl-L-2-pyrrolidinecarboxamido)-1-thio-L- threo -α-D- galacto -octopyranoside 2-(dihydrogen phosphate). "Image Description"

Indications & Usage

Clindamycin Phosphate Topical Solution, 1% is indicated in the treatment of acne vulgaris. In view of the potential for diarrhea, bloody diarrhea and pseudomembranous colitis, the physician should consider whether other agents are more appropriate. (See CONTRAINDICATIONS , WARNINGS and ADVERSE REACTIONS ).

Dosage & Administration

Apply a thin film of clindamycin phosphate topical solution, 1% twice daily to affected area. Keep all liquid dosage forms in containers tightly closed.

Warnings & Precautions
WARNINGS Orally and parenterally administered clindamycin has been associated with severe colitis which may result in patient death. Use of the topical formulation of clindamycin results in absorption of the antibiotic from the skin surface. Diarrhea, bloody diarrhea, and colitis (including pseudomembranous colitis) have been reported with the use of topical and systemic clindamycin. Studies indicate a toxin(s) produced by clostridia is one primary cause of antibiotic-associated colitis. The colitis is usually characterized by severe persistent diarrhea and severe abdominal cramps and may be associated with the passage of blood and mucus. Endoscopic examination may reveal pseudomembranous colitis. Stool culture for Clostridium difficile and stool assay for C. difficile toxin may be helpful diagnostically. When significant diarrhea occurs, the drug should be discontinued. Large bowel endoscopy should be considered to establish a definitive diagnosis in cases of severe diarrhea. Antiperistaltic agents such as opiates and diphenoxylate with atropine may prolong and/or worsen the condition. Vancomycin has been found to be effective in the treatment of antibiotic-associated pseudomembranous colitis produced by Clostridium difficile . The usual adult dosage is 500 milligrams to 2 grams of vancomycin orally per day in three to four divided doses administered for 7 to 10 days. Cholestyramine or colestipol resins bind vancomycin in vitro . If both a resin and vancomycin are to be administered concurrently, it may be advisable to separate the time of administration of each drug. Diarrhea, colitis, and pseudomembranous colitis have been observed to begin up to several weeks following cessation of oral and parenteral therapy with clindamycin.
Contraindications

Clindamycin phosphate topical solution, 1% is contraindicated in individuals with a history of hypersensitivity to preparations containing clindamycin or lincomycin, a history of regional enteritis or ulcerative colitis, or a history of antibiotic-associated colitis.

Adverse Reactions

In 18 clinical studies of various formulations of clindamycin phosphate topical solution using placebo vehicle and/or active comparator drugs as controls, patients experienced a number of treatment emergent adverse dermatologic events [see table below]. Number of Patients Reporting Event Treatment Emergent Adverse Event Solution n=553 (%) Burning 62 (11) Itching 36 (7) Burning/Itching 60 (11) Dryness 105 (19) Erythema 86 (16) Oiliness/Oily Skin 8 (1) Peeling 61 (11) Orally and parenterally administered clindamycin has been associated with severe colitis which may end fatally. Cases of diarrhea, bloody diarrhea and colitis (including pseudomembranous colitis) have been reported as adverse reactions in patients treated with oral and parenteral formulations of clindamycin and rarely with topical clindamycin (see WARNINGS ). Abdominal pain, gastrointestinal disturbances, gram-negative folliculitis, eye pain and contact dermatitis have also been reported in association with the use of topical formulations of clindamycin.


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