Clindamycin Phosphate 10 mg/g Gel — NDC 21922-0027-07 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Clindamycin Phosphate 10 mg/g Gel — NDC 21922-027-07 (Billing 21922-0027-07)

by Encube Ethicals, Inc. · 1 TUBE in 1 CARTON / 60 g in 1 TUBE

This is a package of Clindamycin Phosphate 10 mg/g Gel from Encube Ethicals, Inc., marketed since Mar 2021 and currently FDA-listed; retail pharmacies pay about $0.1307 per g (NADAC). It is the main listing for this product, which comes in 2 package sizes.

NDC 21922-0027-07
🏷️ FDA NDC (as labeled) 21922-027-07 billing pads the product segment with a zero
This package
Contains60 g in 1 tube Cost per g$0.1307 NADAC Per package$7.84 / 60 g Pack sizes2 compare ↓
Also priced by: Medicaid pays $0.3927/unit · Part D plans $0.3596/unit — full pricing hub ↓
Main listing for product 21922-027 · Also comes in: 30 g 21922-027-05
Rx only Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 6, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 21922-027-07
Product NDC 21922-027
11-digit billing NDC 21922002707
NCPDP billing unit GM — per gram (weight)
RxCUI 2676585
UNII EH6D7113I8
Application # ANDA212438
SPL Set ID ac21d7ad-f94e-4d57-95e3-1648add7ad0b
Established class (EPC) Lincosamide Antibacterial
Physiologic effect Decreased Sebaceous Gland Activity; Neuromuscular Blockade
Chemical class Lincosamides
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-03-15
Route TOPICAL
Dosage form GEL
Substance CLINDAMYCIN PHOSPHATE
TE code (Orange Book) AB1 · RLD · RS

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GCN Seq No 007726
GCN 45410
HICL code 004045
Ingredient (HICL) Clindamycin Phosphate
HIC1 code Q
Therapeutic class — broad (HIC1) Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code Q5
Therapeutic class — intermediate (HIC2) Agents Acting Principally On The Skin
HIC3 code Q5W
Therapeutic class — specific (HIC3) Topical Antibiotics
AHFS code 08:12.28.20
AHFS class Lincomycin Antibiotics
FDB label name CLINDAMYCIN PH 1% GEL
FDB brand name Clindamycin Phosphate
Legend status F — Federal legend — prescription drug or device
Quick answers
  • GSN (GCN sequence number): 007726
  • GCN: 45410
  • HICL (First Databank): 004045
  • AHFS class code: 08:12.28.20
  • RxCUI (RxNorm): 2676585
Why two NDCs? The FDA registers this code as 21922-027-07 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 21922-0027-07. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Lincosamide Antibacterial class.

Pharmacologic class Lincosamide Antibacterial
Drug family (ATC) Antiinfectives for treatment of acne, Antibiotics, Lincosamides
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

Label name CLINDAMYCIN PH 1% GEL Ingredient Clindamycin Phosphate
📖 What it is MedlinePlus · NLM

Topical clindamycin is used to treat acne. Clindamycin is in a class of medications called lincomycin antibiotics. It works by slowing or stopping the growth of bacteria that cause acne and by decreasing swelling.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • It treats serious bacterial infections, such as anaerobic infections, skin, lung, abdominal, gynecological, and bone and joint infections, depending on the product. It is often use...
  • Swallow them with a full glass of water and stay upright for at least 30 minutes afterward. This helps prevent irritation of your throat. Take it as often as your prescriber says a...
  • Rash, nausea, vomiting, stomach pain and itching are among the more commonly reported effects. Call your doctor right away if you get severe, watery or bloody diarrhea, even weeks...
  • What side effects are normal, and when should I call you?
📖 Read our full Clindamycin guide →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly $0.131 $7.84 / 60 g
Medicaid paysCMS SDUD · 12 mo $0.3927 $23.56 / 60 g
Medicare drug plans payPart D · Q2 2026 $0.3596 $21.58 / 60 g
NADAC price history (per g) — tap or hover for the price & month
Jan 2022 Aug 2022 Jan 2026 Sep 2026 $0.554 $0.129
▼ Down 76% over the last 24 months.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Per unit Per pack Marketing startMarketing endStatus
21922-0027-05 21922-027-05 1 TUBE in 1 CARTON / 30 g in 1 TUBE $0.1424 / g $4.27 2020-01-13 — Active
21922-0027-07 You're viewing this Main listing 1 TUBE in 1 CARTON / 60 g in 1 TUBE $0.1307 / g $7.84 2020-01-13 — Active

This pack has the lowest per-g cost of the 2 priced pack sizes ($0.1307 NADAC).

In Medicaid, this is the most-dispensed pack of this product — about 57% of fills over the last four reported quarters. See all packs ↓

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 tube in 1 carton / 60 g in 1 tube.
What NDC number is used to bill for this package of Clindamycin Phosphate 10 mg/g Gel?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Prices are the latest CMS NADAC pharmacy acquisition cost per NDC; per-pack figures are per-unit × pack quantity, shown only when the pack is denominated in the same measure NADAC prices.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Clindamycin Phosphate 10 mg/gthis 21922-0027-07 Encube 1 tube $0.131 AB1 Availability likely —
clindamycin phosphate 10 mg/g 00168-0202-30 E. 1 tube $0.142 AB1 Availability likely +9%
Clindamycin Phosphate 10 mg/g 16714-0161-01 NORTHSTAR 1 tube $0.142 AB1 Availability likely +9%
Clindamycin Phosphate 10 mg/g 45802-0900-94 Padagis 1 tube $0.142 AB1 Availability likely +9%
Clindamycin Phosphate 10 mg/g 51672-1399-02 Sun 1 tube $0.142 AB1 Availability likely +9%
clindamycin phosphate 10 mg/g 59762-3743-01 Mylan 1 tube $0.142 AB1 Availability likely +9%
Clindamycin Phosphate 10 mg/g 62332-0623-30 Alembic 1 tube $0.142 AB1 Availability likely +9%
Clindamycin Phosphate 10 mg/g 68462-0866-35 GLENMARK 1 tube $0.142 AB1 Availability likely +9%
Clindamycin Phosphate 10 mg/g 72578-0118-01 Viona 1 tube $0.142 AB1 Availability likely +9%
Clindamycin Phosphate 10 mg/g 73473-0300-30 Solaris 1 tube $0.142 AB1 Availability likely +9%
Clindamycin Phosphate 10 mg/g 46708-0623-30 Alembic 1 tube — AB1 FDA listed —
Clindamycin Phosphate 10 mg/g 50090-5958-00 A-S 1 tube — AB1 FDA listed —
Clindamycin Phosphate 10 mg/g 50090-6072-00 A-S 1 tube — AB1 FDA listed —
Clindamycin Phosphate 10 mg/g 59651-0806-30 Aurobindo 1 tube — AB1 FDA listed —
Clindamycin Phosphate 10 mg/g 63629-8630-01 Bryant 1 tube — AB1 FDA listed —
Clindamycin Phosphate 10 mg/g 63629-8631-01 Bryant 1 tube — AB1 FDA listed —
Clindamycin Phosphate 10 mg/g 63629-9309-01 Bryant 1 tube — AB1 FDA listed —
Clindamycin Phosphate 10 mg/g 68788-8423-06 Preferred 1 tube — AB1 FDA listed —
Clindamycin Phosphate 10 mg/g 70771-1855-02 Zydus 1 tube — AB1 FDA listed —
Clindamycin Phosphate 10 mg/g 72162-1436-06 Bryant 1 tube — AB1 FDA listed —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2021
On the market since
Mar 2021
📍
2026
Currently FDA-listed
5 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII HHT01ZNK31
    Carbomer Homopolymer Type B is a synthetic polymer made from acrylic acid. It absorbs water and forms a gel, so it's used in medicines as a thickener, suspending agent, and to help create a smooth texture in creams, gels, and lotions.
  • UNII A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • UNII B697894SGQ
    Polyethylene glycol 400 is a clear, thick liquid made from petroleum-derived polymers. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

7 inactive ingredients listed in the exact product block matched to this NDC.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerEncube Ethicals, Inc.
Application holderENCUBE ETHICALS PRIVATE LTD
FDA applicationANDA212438 (ANDA)
Labeler code21922
First marketedMar 2021
Product typeHuman Prescription Drug
Portfolio77 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

Full prescribing information FDA SPL

The complete FDA label for this product — the official prescribing information, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage 46 words ▾

INDICATIONS AND USAGE Clindamycin phosphate gel USP, 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 and Administration 20 words ▾

DOSAGE AND ADMINISTRATION Apply a thin film of clindamycin phosphate gel twice daily to affected area. Keep container tightly closed.

⛔ Contraindications 33 words ▾

CONTRAINDICATIONS Clindamycin phosphate gel 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.

⚠️ Warnings ~1 min read ▾

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 systemic absorption 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 Clostridioides 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 Clostridioides 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.

🤒 Adverse Reactions 150 words ▾

ADVERSE REACTIONS In 18 clinical studies of various formulations of clindamycin phosphate 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 Events Treatment Emergent Adverse Event Gel n= 148(%) Burning 15 (10) Itching 15 (10) Burning/Itching # ( – ) Dryness 34 (23) Erythema 10 ( 7) Oiliness/Oily Skin 26 (18) Peeling # ( – ) # not recorded 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.

🔄 Drug Interactions 33 words ▾

Drug Interactions Clindamycin has been shown to have neuromuscular blocking properties that may enhance the action of other neuromuscular blocking agents. Therefore, it should be used with caution in patients receiving such agents.

🤰 Pregnancy 59 words ▾

Pregnancy: Teratogenic effects In clinical trials with pregnant women, the systemic administration of clindamycin during the second and third trimesters has not been associated with an increased frequency of congenital abnormalities. There are no adequate studies in pregnant women during the first trimester of pregnancy. Clindamycin should be used during the first trimester of pregnancy only if clearly needed.

🧒 Pediatric Use 17 words ▾

Pediatric Use Safety and effectiveness in pediatric patients under the age of 12 have not been established.

🧓 Geriatric Use 43 words ▾

Geriatric Use Clinical studies for clindamycin phosphate did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients.

🆘 Overdosage 18 words ▾

OVERDOSAGE Topically applied clindamycin phosphate can be absorbed in sufficient amounts to produce systemic effects (see WARNINGS ).

🧬 Clinical Pharmacology 189 words ▾

CLINICAL PHARMACOLOGY Mechanism of Action The mechanism of action of clindamycin in treating acne vulgaris is unknown. Pharmacokinetics Following multiple topical applications of clindamycin phosphate at a concentration equivalent to 10 mg clindamycin per mL in an isopropyl alcohol and water solution, very low levels of clindamycin are present in the serum (0 to 3 ng/mL) and less than 0.2% of the dose is recovered in urine as clindamycin. Although clindamycin phosphate is inactive in vitro , rapid i n vivo hydrolysis converts this compound to the antibacterially active clindamycin.

Microbiology Clindamycin inhibits bacterial protein synthesis by binding to the 23S RNA of the 50S subunit of the ribosome. Clindamycin is bacteriostatic. Antimicrobial Activity Clindamycin is active in vitro against most isolates of Propionibacterium acnes ; however, the clinical significance is unknown.

Resistance Resistance to clindamycin is most often caused by modification of specific bases of the 23S ribosomal RNA. Cross-resistance between clindamycin and lincomycin is complete. Because the binding sites for these antibacterial drugs overlap, cross resistance is sometimes observed among lincosamides, macrolides and streptogramin B.

Macrolide‑ inducible resistance to clindamycin occurs in some isolates of macrolide-resistant bacteria.

📦 How Supplied / Storage and Handling 129 words ▾

HOW SUPPLIED Clindamycin phosphate gel USP, 1% containing clindamycin phosphate equivalent to 10 mg clindamycin per gram is available in the following sizes: 60 gram tube - NDC 21922-027-07 30 gram tube- NDC 21922-027-05 To report SUSPECTED ADVERSE REACTIONS, contact Encube Ethicals Private Limited at 1-833-285-4151 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. Store at 20°C to 25°C (68°F to 77°F) [see USP Controlled Room Temperature]. Protect from freezing.

Rx only Manufacture by: Encube Ethicals Pvt. Ltd. Plot No.

113, Smart Industrial Park, Pithampur, District: Dhar – 454 774, Madhya Pradesh, India. OR Manufacture by: Encube Ethicals Pvt. Ltd.

Plot No. C-1, Madkaim Industrial Estate, Madkaim, Post. Mardol, Ponda, Goa – 403 404, India.

Distributed by: Encube Ethicals, Inc. 200 Meredith Drive, Suite 202, Durham, NC 27713 USA Revised: 05/2026

📋 Description 89 words ▾

DESCRIPTION Clindamycin phosphate gel USP, 1% contains clindamycin phosphate, USP, at a concentration equivalent to 10 mg clindamycin per gram. Clindamycin phosphate is a water soluble ester of the semi-synthetic antibacterial drug produced by a 7(S)-chloro-substitution of the 7(R)-hydroxyl group of the parent compound lincomycin. The gel contains allantoin, carbopol 974 P, methylparaben, polyethylene glycol 400, 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). structure

⚠️ Precautions ~1 min read ▾

PRECAUTIONS General Clindamycin phosphate should be prescribed with caution in atopic individuals. Drug Interactions Clindamycin has been shown to have neuromuscular blocking properties that may enhance the action of other neuromuscular blocking agents. Therefore, it should be used with caution in patients receiving such agents.

Pregnancy: Teratogenic effects In clinical trials with pregnant women, the systemic administration of clindamycin during the second and third trimesters has not been associated with an increased frequency of congenital abnormalities. There are no adequate studies in pregnant women during the first trimester of pregnancy. Clindamycin should be used during the first trimester of pregnancy only if clearly needed.

Nursing Mothers It is not known whether clindamycin is excreted in breast milk following use of clindamycin phosphate. However, orally and parenterally administered clindamycin has been reported to appear in breast milk. Clindamycin has the potential to cause adverse effects on the breast-fed infant's gastrointestinal flora.

Monitor the breast-fed infant for possible adverse effects on the gastrointestinal flora, such as diarrhea, candidiasis (thrush, diaper rash) or rarely, blood in the stool indicating possible antibiotic-associated colitis. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for clindamycin and any potential adverse effects on the breast-fed child from clindamycin or from the underlying maternal condition. Clinical Considerations If used during lactation and clindamycin phosphate is applied to the chest, care should be taken to avoid accidental ingestion by the infant.

Pediatric Use Safety and effectiveness in pediatric patients under the age of 12 have not been established. Geriatric Use Clinical studies for clindamycin phosphate did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients.

🍼 Nursing Mothers 135 words ▾

Nursing Mothers It is not known whether clindamycin is excreted in breast milk following use of clindamycin phosphate. However, orally and parenterally administered clindamycin has been reported to appear in breast milk. Clindamycin has the potential to cause adverse effects on the breast-fed infant's gastrointestinal flora.

Monitor the breast-fed infant for possible adverse effects on the gastrointestinal flora, such as diarrhea, candidiasis (thrush, diaper rash) or rarely, blood in the stool indicating possible antibiotic-associated colitis. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for clindamycin and any potential adverse effects on the breast-fed child from clindamycin or from the underlying maternal condition. Clinical Considerations If used during lactation and clindamycin phosphate is applied to the chest, care should be taken to avoid accidental ingestion by the infant.

📄 Package Label / Principal Display Panel ~1 min read ▾

PRINCIPAL DISPLAY PANEL - 30GM PACK Clindamycin Phosphate Gel USP, 1% - 30GM Pack Carton Label (30 GM): NDC 21922- 027 -05 Clindamycin Phosphate Gel USP, 1% For topical use only 30 gram Rx only Manufacture by: Encube Ethicals Pvt. Ltd. Plot No.

C-1, Madkaim Industrial Estate, Madkaim, Post. Mardol, Ponda, Goa – 403 404, India. Distributed by: Encube Ethicals, Inc.

200 Meredith Drive, Suite 202, Durham, NC 27713 USA. Carton Label (30 GM): NDC 21922- 027 -05 Clindamycin Phosphate Gel USP, 1% For topical use only 30 gram Rx only Manufacture by: Encube Ethicals Pvt. Ltd.

Plot No. 113, Smart Industrial Park, Pithampur, District: Dhar – 454 774, Madhya Pradesh, India. Distributed by: Encube Ethicals, Inc.

200 Meredith Drive, Suite 202, Durham, NC 27713 USA. carton-30g-goa carton-30g-indore

PRINCIPAL DISPLAY PANEL -60 GM PACK Clindamycin Phosphate Gel USP, 1% - 60GM Pack Carton Label (60 GM): NDC 21922- 027 -07 Clindamycin Phosphate Gel USP, 1% For topical use only 60 gram Rx only Manufacture by: Encube Ethicals Pvt. Ltd. Plot No.

C-1, Madkaim Industrial Estate, Madkaim, Post. Mardol, Ponda, Goa – 403 404, India. Distributed by: Encube Ethicals, Inc.

200 Meredith Drive, Suite 202, Durham, NC 27713 USA. Carton Label (60 GM): NDC 21922- 027 -07 Clindamycin Phosphate Gel USP, 1% For topical use only 60 gram Rx only Manufacture by: Encube Ethicals Pvt. Ltd.

Plot No. 113, Smart Industrial Park, Pithampur, District: Dhar – 454 774, Madhya Pradesh, India. Distributed by: Encube Ethicals, Inc.

200 Meredith Drive, Suite 202, Durham, NC 27713 USA. carton-60g-goa carton-60g-indore

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Medicaid utilization & spend

📍 This exact package only: Medicaid data is reported per full 11-digit NDC — labeler, product and pack size — so every number here is for this package alone, not the drug overall. Other pack sizes report separately.
💊 Pharmacy benefit only: These are Medicaid outpatient pharmacy claims, billed by NDC. They exclude the medical benefit — clinic- or hospital-administered drugs billed under HCPCS J-codes — so drugs used mostly that way (e.g. Avastin, Lucentis, Keytruda) can look low or missing here. That’s expected, not an error.
📅 Q1 2025 – Q1 2026 · 5 quarters of data
ⓘ The newest quarter is usually incomplete when first published; states restate recent quarters in later CMS releases, so the latest figures typically revise upward. State coverage-policy changes can also shift quarter-to-quarter totals.
Prescriptions last 4 qtrs
159.1K
Units reimbursed last 4 qtrs
9.6M
Gross reimbursed last 4 qtrs
$3.77M
Avg / prescription
$23.67
Avg / unit
$0.3927
Latest quarter Q1 2026
38.3KRx
Medicaid pays / g
$0.3927
gross reimbursed
vs
NADAC / g
$0.1307
acquisition cost
=
Spread
+$0.2620
+200% vs cost
What Medicaid paid per g (before rebates; includes the pharmacy’s dispensing fee) compared with NADAC — the average price pharmacies pay to buy the drug. A positive spread means Medicaid reimbursed more than the purchase price, before manufacturer rebates.
Fee-for-service vs managed care ⓘ
51% FFS 49% MCO
Fee-for-service · 80,775 Rx Managed care · 78,353 Rx
State Medicaid map
Alaska: 2,460 units · 336 per 100k residents AK Maine: 28,740 units · 2,060 per 100k residents ME Washington: 30,142 units · 386 per 100k residents WA Idaho: 50,250 units · 2,559 per 100k residents ID Montana: 15,210 units · 1,344 per 100k residents MT North Dakota: 8,400 units · 1,073 per 100k residents ND Minnesota: 226,252 units · 3,944 per 100k residents MN Wisconsin: 400,470 units · 6,776 per 100k residents WI Michigan: 30,480 units · 304 per 100k residents MI New York: 2,092,401 units · 10,691 per 100k residents NY Vermont: 8,250 units · 1,275 per 100k residents VT New Hampshire: 30,540 units · 2,178 per 100k residents NH Oregon: 38,460 units · 909 per 100k residents OR Nevada: 96,660 units · 3,026 per 100k residents NV Wyoming: no data reported WY South Dakota: 24,450 units · 2,661 per 100k residents SD Iowa: 85,020 units · 2,651 per 100k residents IA Illinois: 299,430 units · 2,386 per 100k residents IL Indiana: 122,940 units · 1,792 per 100k residents IN Ohio: 283,740 units · 2,408 per 100k residents OH Pennsylvania: 281,880 units · 2,175 per 100k residents PA New Jersey: 31,800 units · 342 per 100k residents NJ Massachusetts: 691,156 units · 9,872 per 100k residents MA California: 1,429,487 units · 3,669 per 100k residents CA Utah: 18,180 units · 532 per 100k residents UT Colorado: 28,170 units · 479 per 100k residents CO Nebraska: no data reported NE Missouri: 119,700 units · 1,932 per 100k residents MO Kentucky: 325,598 units · 7,194 per 100k residents KY West Virginia: no data reported WV Virginia: 147,855 units · 1,696 per 100k residents VA Maryland: 218,130 units · 3,530 per 100k residents MD Connecticut: 65,580 units · 1,813 per 100k residents CT Rhode Island: 10,560 units · 964 per 100k residents RI Arizona: 154,470 units · 2,079 per 100k residents AZ New Mexico: 94,470 units · 4,469 per 100k residents NM Kansas: 12,420 units · 422 per 100k residents KS Arkansas: no data reported AR Tennessee: 204,090 units · 2,864 per 100k residents TN North Carolina: 216,060 units · 1,994 per 100k residents NC South Carolina: 13,020 units · 242 per 100k residents SC Delaware: 9,120 units · 885 per 100k residents DE Oklahoma: 102,805 units · 2,537 per 100k residents OK Louisiana: 69,660 units · 1,523 per 100k residents LA Mississippi: 36,000 units · 1,224 per 100k residents MS Alabama: no data reported AL Georgia: 581,220 units · 5,270 per 100k residents GA D.C.: 13,740 units · 2,024 per 100k residents DC Hawaii: 10,050 units · 700 per 100k residents HI Texas: 596,415 units · 1,955 per 100k residents TX Florida: 235,875 units · 1,043 per 100k residents FL
Units reimbursed · per 100k residents
24210,691
gray = no data reported ⓘ
Colors are per 100,000 residents, so big states don’t automatically dominate. Tap or hover a state for its actual totals.
Tap or hover a state
…for its Medicaid breakdown
🏆 Top states by units · per 100k residents
1 New York 10,691 /100k
2 Massachusetts 9,872 /100k
3 Kentucky 7,194 /100k
4 Wisconsin 6,776 /100k
5 Georgia 5,270 /100k
6 New Mexico 4,469 /100k
7 Minnesota 3,944 /100k
8 California 3,669 /100k
National units — by quarter
💵 About the dollar figures: “reimbursed” is what Medicaid paid pharmacies before confidential manufacturer rebates, so the program’s real net cost is lower than these numbers. Fee-for-service and managed-care claims are combined unless split above. Source: CMS State Drug Utilization Data; per-100k rates use 2023 Census population estimates.

Medicaid utilization by pack size

Medicaid (SDUD) totals over the four most recent reported quarters for every package size of this drug — handy when a specific package (e.g. a starter/titration pack) carries little or no Medicaid volume on its own.
1 tube this page21922-0027-07 159,128 Rx · $3,766,737
1 tube21922-0027-05 117,893 Rx · $2,059,789
Drug total (last 4 qtrs): 277,021 Rx · 13,737,023 units · $5,826,526 gross reimbursed
Tap a pack size to open its page. Source: CMS State Drug Utilization Data, last 4 quarters.

Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Clindamycin Phosphate — the program that covers self-administered drugs. 16 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Clindamycin Phosphate. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$6.9M
Claims incl. refills
181.3K
Beneficiaries
134.5K
Spend / beneficiary
$51.31
Spend / claim
$38.08
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Clindamycin Phosphate Topical — the ingredient across all brands.

Top reported reactions

Rash252
Drug Hypersensitivity228
Diarrhoea188
Nausea180
Fatigue166
Pain158
Pruritus157

Age at onset

Neonate11
Infant5
Child12
Adolescent40
Adult320
Elderly114

Reporter sex

3,472 reports
Male · 36%
Female · 64%
Unknown · 0%

Serious outcomes

Hospitalization1,027
Death263
Life-threatening207
Disabling72
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 307 161
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.