PROCTOFOAM

Manufacturer
Viatris Specialty LLC
Effective date
2025-04-15
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-05-31 21:41:03

Label at a glance#

ProductPROCTOFOAM HC
Active ingredientPRAMOXINE HYDROCHLORIDE, HYDROCORTISONE ACETATE
Label structure12 sections

Indications and uses

Proctofoam ® HC is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses of the anal region.

Dosage and administration

Apply to affected area 3 to 4 times daily. Use the applicator supplied for anal administration. For perianal use, transfer a small quantity to a tissue and rub in gently. Directions for Use. 1. Attach Cap: Place cap on top of container. 2. Shake Container: Shake foam container vigorously for 5-10 seconds before each use. Do not remove container cap during use of the product. 3. Attach Applicator: Hold container up...

Label contents#

Full prescribing information#

DESCRIPTION

DESCRIPTION SECTION

Proctofoam® HC (hydrocortisone acetate 1% and pramoxine hydrochloride 1%) is a topical aerosol foam for anal use containing hydrocortisone acetate 1% and pramoxine hydrochloride 1% in a hydrophilic base containing cetyl alcohol, emulsifying wax, methylparaben, poly-oxyethylene-10-stearyl ether, propylene glycol, propylparaben, purified water, trolamine and inert propellants: isobutane and propane.

Proctofoam® HC contains a synthetic corticosteroid used as an anti-inflammatory/antipruritic agent and a local anesthetic.

Hydrocortisone acetate

Molecular weight: 404.50. Solubility of hydrocortisone acetate in water: 1 mg/100 mL.

Chemical name: pregn-4-ene-3,20-dione, 21-(acetyloxy)-11,17-dihydroxy-,(11β)-.

Hydrocortisone Acetate Structural Formula
Hydrocortisone Acetate Structural Formula

Pramoxine hydrochloride

Molecular weight: 329.86. Pramoxine hydrochloride is freely soluble in water. Chemical name: morpholine, 4-[3-(4-butoxyphenoxy) propyl]-, hydrochloride.

Pramoxine Hydrochloride Structural Formula
Pramoxine Hydrochloride Structural Formula

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Topical corticosteroids share anti-inflammatory, antipruritic and vasoconstrictive actions.

The mechanism of anti-inflammatory activity of the topical corticosteroids is unclear. Various laboratory methods, including vasoconstrictor assays, are used to compare and predict potencies and/or clinical efficacies of the topical corticosteroids. There is some evidence to suggest that a recognizable correlation exists between vasoconstrictor potency and therapeutic efficacy in man.

Pramoxine hydrochloride is a surface or local anesthetic which is not chemically related to the "caine" types of local anesthetics. Its unique chemical structure is likely to minimize the danger of cross-sensitivity reactions in patients allergic to other local anesthetics.

Pharmacokinetics

PHARMACOKINETICS SECTION

The extent of percutaneous absorption of topical corticosteroids is determined by many factors including the vehicle, the integrity of the epidermal barrier, and the use of occlusive dressings.

Topical corticosteroids can be absorbed through normal intact skin. Inflammation and/or other disease processes in the skin increase the percutaneous absorption of topical corticosteroids. Occlusive dressings substantially increase the percutaneous absorption of topical corticosteroids. Thus, occlusive dressings may be a valuable therapeutic adjunct for treatment of resistant dermatoses. (See DOSAGE AND ADMINISTRATION.)

Once absorbed through the skin, topical corticosteroids are handled through pharmacokinetic pathways similar to systemically administered corticosteroids. Corticosteroids are bound to plasma proteins in varying degrees. Corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys. Some of the topical corticosteroids and their metabolites are also excreted into the bile.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Proctofoam® HC is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses of the anal region.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

Topical corticosteroid products are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.

WARNINGS

WARNINGS SECTION

Do not insert any part of the aerosol container directly into the anus. Avoid contact with the eyes. Contents of the container are under pressure. Do not burn or puncture the aerosol container. Do not store at temperatures above 120°F (49°C). If there is no evidence of clinical improvement within two or three weeks after starting Proctofoam® HC therapy, or if the patient's condition worsens, discontinue the drug. Keep this and all medicines out of the reach of children.

PRECAUTIONS

PRECAUTIONS SECTION

General

GENERAL PRECAUTIONS SECTION

Systemic absorption of topical corticosteroids has produced reversible hypothalamic-pituitary-adrenal (HPA) axis suppression, manifestations of Cushing's syndrome, hyperglycemia, and glucosuria in some patients.

Conditions which augment systemic absorption include the application of the more potent steroids, use over large surface areas, prolonged use, and the addition of occlusive dressings. Therefore, patients receiving a large dose of a potent topical steroid applied to a large surface area or under an occlusive dressing should be evaluated periodically for evidence of HPA axis suppression by using the urinary free cortisol and ACTH stimulation tests. If HPA axis suppression is noted, an attempt should be made to withdraw the drug, to reduce the frequency of application or to substitute a less potent steroid.

Recovery of HPA axis function is generally prompt and complete upon discontinuation of the drug. Infrequently, signs and symptoms of steroid withdrawal may occur, requiring supplemental systemic corticosteroids. Pediatric patients may absorb proportionally larger amounts of topical corticosteroids and thus be more susceptible to systemic toxicity. (see PRECAUTIONS: Pediatric Use.)

If irritation develops, topical corticosteroids should be discontinued and appropriate therapy instituted.

In the presence of dermatological infections, the use of an appropriate antifungal or antibacterial agent should be instituted. If a favorable response does not occur promptly, the corticosteroid should be discontinued until the infection has been adequately controlled.

Information for the Patient

SPL UNCLASSIFIED SECTION

Patients using topical corticosteroids should receive the following information and instructions:

  1. This medication is to be used as directed by the physician. It is for anal or perianal use only. Avoid contact with eyes.
  2. Be advised not to use this medication for any disorder other than for which it has been prescribed.
  3. Report any signs of adverse reactions.

Laboratory Tests

LABORATORY TESTS SECTION

The following tests may be helpful in evaluating the HPA axis suppression:

Urinary free cortisol test

ACTH stimulation test

Carcinogenesis, Mutagenesis, Impairment of Fertility

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION

Long-term animal studies have not been performed to evaluate the carcinogenic potential or the effect on fertility of topical corticosteroids.

Studies to determine mutagenicity with prednisolone and hydrocortisone have revealed negative results.

Pregnancy

PREGNANCY SECTION

Teratogenic Effects

TERATOGENIC EFFECTS SECTION

Corticosteroids are generally teratogenic in laboratory animals when administered systemically at relatively low dosage levels. The more potent corticosteroids have been shown to be teratogenic after dermal application in laboratory animals. There are no adequate, well-controlled studies of teratogenic effects from topically applied corticosteroids in pregnant women. Therefore, topical corticosteroids should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Drugs of this class should not be used extensively on pregnant patients, in large amounts, or for prolonged periods of time.

Nursing Mothers

NURSING MOTHERS SECTION

It is not known whether topical administration of corticosteroids could result in sufficient systemic absorption to produce detectable quantities in breast milk. Systemically administered corticosteroids are secreted into breast milk in quantities not likely to have a deleterious effect on the infant. Nevertheless, caution should be exercised when topical corticosteroids are administered to a nursing woman.

Pediatric Use

PEDIATRIC USE SECTION

Pediatric patients may demonstrate greater susceptibility to topical corticosteroid-induced HPA axis suppression and Cushing's syndrome than mature patients because of a larger skin surface area to body weight ratio.

Hypothalamic-pituitary-adrenal (HPA) axis suppression, Cushing's syndrome, and intracranial hypertension have been reported in pediatric patients receiving topical corticosteroids. Manifestations of adrenal suppression in pediatric patients include linear growth retardation, delayed weight gain, low plasma cortisol levels, and absence of response to ACTH stimulation. Manifestations of intracranial hypertension include bulging fontanelles, headaches, and bilateral papilledema.

Administration of topical corticosteroids to pediatric patients should be limited to the least amount compatible with an effective therapeutic regimen. Chronic corticosteroid therapy may interfere with the growth and development of pediatric patients.

Geriatric Use

GERIATRIC USE SECTION

Reported clinical experience has not identified differences in responses between the elderly and younger patients. In general, dose selection for an elderly patient should be cautious using the least amount compatible with an effective therapeutic regimen and reflecting the greater frequency of decreased hepatic, renal or cardiac function, and of concomitant disease or other drug therapy.

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

The following local adverse reactions are reported infrequently with topical corticosteroids, but may occur more frequently with the use of occlusive dressings. These reactions are listed in approximate decreasing order of occurrence: burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infection, skin atrophy, striae and miliaria.

To report SUSPECTED ADVERSE REACTIONS, contact Meda Pharmaceuticals Inc. at 1-866-210-5948 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

OVERDOSAGE

OVERDOSAGE SECTION

Topically applied corticosteroids can be absorbed in sufficient amounts to produce systemic effects. (See PRECAUTIONS.)

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Apply to affected area 3 to 4 times daily. Use the applicator supplied for anal administration. For perianal use, transfer a small quantity to a tissue and rub in gently.

Directions for Use.

  1. Attach Cap: Place cap on top of container.
  2. Shake Container: Shake foam container vigorously for 5-10 seconds before each use. Do not remove container cap during use of the product.
  3. Attach Applicator: Hold container upright on a level surface and gently place the tip of the applicator onto the nose of the container cap. CONTAINER MUST BE HELD UPRIGHT TO OBTAIN PROPER FLOW OF MEDICATION.
  4. Pull Plunger: Pull plunger past the fill line on the applicator barrel.
  5. Prime Container: Hold the container and applicator at eye level. Place the index and middle fingers on the container cap flanges and the thumb beneath the container. Support the applicator with your other hand. Prime the container by pressing down firmly on flanges and then release. With initial priming, a burst of air may come out of the container. It usually requires 1-2 pumps for foam to appear.
  6. Fill Applicator: To fill applicator barrel, press down firmly on cap flanges, hold for 1-2 seconds, and release. Wait 5-10 seconds to allow foam to expand in applicator barrel. Repeat until foam reaches fill line. It usually requires 3-4 pumps for foam to reach fill line. Remove applicator from container cap. Note: If foam goes beyond fill line, it will continue to expand and flow backwards resulting in foam build-up under cap.
  7. Foam Application: Hold applicator firmly by barrel, making sure thumb and middle finger are positioned securely underneath and resting against barrel wings. Place index finger over the plunger. Gently insert tip into anus. Once in place, push plunger to expel foam, then withdraw applicator. CAUTION: Do not insert any part of the aerosol container directly into the anus. Apply to anus only with enclosed applicator. Do not insert any part of the applicator past the anus into rectum.
  8. Clean Applicator: After each use, applicator parts should be pulled apart for thorough cleaning with warm water. Since some foam will appear under the cap, the cap and underlying tip should be pulled apart and rinsed to help prevent build-up of foam and possible blockage.

HOW SUPPLIED

HOW SUPPLIED SECTION

Proctofoam® HC is supplied in an aerosol container with a special anal applicator. When used correctly, the aerosol container will deliver a minimum of 14 applications.

NDC 0037-6822-10     10 g

Store upright at controlled room temperature 20°-25°C (68°-77°F). DO NOT REFRIGERATE.

Distributed by:
Meda Pharmaceuticals Inc.
Canonsburg, PA 15317 U.S.A.

© 2025 Viatris Inc.

PROCTOFOAM is a registered trademark of Alaven Pharmaceutical LLC, a Viatris Company.

IN-682210-05

141371-0421

Patient Instructions

INSTRUCTIONS FOR USE SECTION

PLEASE READ CAREFULLY BEFORE USING

 

PATIENT INSTRUCTIONS FOR

proctofoam® HC

(hydrocortisone acetate 1% and
pramoxine hydrochloride 1%)

IFU Figure 1IFU Figure 1

TOPICAL AEROSOL

Keep this insert. It contains

important information about

the use of proctofoam® HC.

 

 

IFU Figure 2IFU Figure 2
  1. Attach Cap: Place cap on top of container.
IFU Figure 3IFU Figure 3
  1. Shake Container: Shake foam container vigorously for 5-10 seconds before each use. Do not remove container cap during use of the product.
IFU Figure 4IFU Figure 4
  1. Attach Applicator: Hold container upright on a level surface and gently place the tip of the applicator onto the nose of the container cap. CONTAINER MUST BE HELD UPRIGHT TO OBTAIN PROPER FLOW OF MEDICATION.
IFU Figure 5IFU Figure 5
  1. Pull Plunger: Pull plunger past the fill line on the applicator barrel.
IFU Figure 6IFU Figure 6
  1. Prime Container: Hold the container and applicator at eye level. Place the index and middle fingers on the container cap flanges and the thumb beneath the container. Support the applicator with your other hand. Prime the container by pressing down firmly on flanges and then release. With initial priming, a burst of air may come out of the container. It usually requires 1-2 pumps for foam to appear.
  1. Fill Applicator: To fill applicator barrel, press down firmly on cap flanges, hold for 1-2 seconds, and release. Wait 5-10 seconds to allow foam to expand in applicator barrel. Repeat until foam reaches fill line. It usually requires 3-4 pumps for foam to reach fill line. Remove applicator from container cap. Note: If foam goes beyond fill line, it will continue to expand and flow backwards resulting in foam build-up under cap.
IFU Figure 7IFU Figure 7
  1. Foam Application: Hold applicator firmly by barrel, making sure thumb and middle finger are positioned securely underneath and resting against barrel wings. Place index finger over the plunger. Gently insert tip into anus. Once in place, push plunger to expel foam, then withdraw applicator. CAUTION: Do not insert any part of the aerosol container directly into the anus. Apply to anus only with enclosed applicator. Do not insert any part of the applicator past the anus into rectum.
IFU Figure 8IFU Figure 8
  1. Clean Applicator: After each use, applicator parts should be pulled apart for thorough cleaning with warm water. Since some foam will appear under the cap, the cap and underlying tip should be pulled apart and rinsed to help prevent build-up of foam and possible blockage.

IS-682210-05

141370-0423

Distributed by:
Meda Pharmaceuticals Inc.

Canonsburg, PA 15317 U.S.A.

 

PROCTOFOAM is a registered trademark of Alaven Pharmaceutical LLC, a Viatris Company.

 

To report SUSPECTED ADVERSE REACTIONS, contact Meda Pharmaceuticals Inc. at 1-866-210-5948 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

PRINCIPAL DISPLAY PANEL - 10 g

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0037-6822-10
STORE UPRIGHT

proctofoam® HC

(hydrocortisone acetate 1% and
pramoxine hydrochloride 1%)
topical aerosol

Rx Only

10 g net wt

Description
proctofoam® HC (hydrocortisone acetate 1% and
pramoxine hydrochloride 1%) is a topical aerosol foam for
anal use containing hydrocortisone acetate 1% and
pramoxine hydrochloride 1% in a hydrophilic base
containing cetyl alcohol, emulsifying wax, methylparaben
polyoxyethylene-10-stearyl ether, propylene glycol
propylparaben, purified water, trolamine, and inert
propellants: isobutane and propane.

Dosage: Apply to affected areas 3 to 4 times daily. Use
the applicator supplied for anal administration. For
perianal use, transfer a small quantity to a tissue and rub
gently. See patient instructions (inside) for full
directions for use. 
Please see package insert for
complete prescribing information.

Caution: Do not insert any part of the aerosol container
directly into the anus. Apply to anus only with the
enclosed applicator. Do not insert any part of applicator
past the anus into rectum.

WARNINGS: Contents of the container are under
pressure. Do not burn or puncture the aerosol container.
Do not store at temperatures above 120°F (49°C).

KEEP OUT OF REACH OF CHILDREN.

Store upright at controlled room temperature
20° - 25°C (68° - 77°F).

DO NOT REFRIGERATE.

117779-2421     UC-682210-07

Distributed by:
Meda Pharmaceuticals Inc
Canonsburg, PA 15317 U.S.A

©2025 Viatris Inc.
PROCTOFOAM is a registered
trademark of
Alaven Pharmaceutical LLC,
a Viatris company.

Proctofoam HC Topical Aerosol 10 g Carton Label
Proctofoam HC Topical Aerosol 10 g Carton Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
828362hydrocortisone acetate 1 % / pramoxine HCl 1 % Rectal FoamPSN10
828364proctofoam-HC 1 % / 1 % Rectal FoamPSN10
828364hydrocortisone acetate 10 MG/ML / pramoxine hydrochloride 10 MG/ML Rectal Foam [Proctofoam-HC]SBD10
828362hydrocortisone acetate 10 MG/ML / pramoxine hydrochloride 10 MG/ML Rectal FoamSCD10
828362hydrocortisone acetate 1 % / pramoxine hydrochloride 1 % Rectal FoamSY10
828364Proctofoam-HC (hydrocortisone acetate 1 % / pramoxine hydrochloride 1 % ) Rectal FoamSY10

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
HYDROCORTISONE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
15bd4439-874a-4934-9954-248e5455d460Product name120260310
9962b773-9f2e-22cc-0032-535e48ac417bProduct name320250724
56bb0587-1bf2-48b2-9d93-fc9f59d1eeb2Product name120250325
4d56e8eb-d741-d4a5-de3f-2bab1af75a60Product name720220608
626d7260-31b5-4412-84fd-579746adb6b3Product name120210513
8a011600-5e61-4c59-ab7b-54ab658a3b71Product name220181127
a919621a-248d-3c7a-1084-9f9ce286fdfdProduct name220181009
e7d5a174-836b-a0af-b014-cb0826c69ddcProduct name220181004
fcce390d-6460-4701-87cf-940d8800a1c3Product name220180212
bf065fa6-1e3b-e4c3-0bde-2dc842ceeea1Product name220150218
02657a3f-1489-66ea-f740-5ab9524e57d7Product name120140508
26f3d783-2cc1-4327-e77d-71804cf675a2Product name120140508
36fdc54c-bbeb-981e-8a53-4d768e283892Product name120140508
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8Product name120140508
61e59a42-186b-9f4b-aec3-fb49a6debc31Product name120140508
705740e1-dee5-2610-c5a3-4c59cd9d62afProduct name120140508
7bdc4804-3832-c0df-e519-72b6d47c9792Product name120140508
a7051cba-790b-a699-81f8-dbbbdbd9b5acProduct name120140508
abaf203f-619e-f265-559f-8c81af5cb1c2Product name120140508
acc4d8bb-0e29-e9f8-65f8-31e94184a9c0Product name120140508
b045ad64-0f28-9a02-2f9b-b34d94fb2278Product name120140508
bfd28ffb-d550-3fe9-f65b-10bcb7f971fdProduct name120140508
da108d9e-edc8-17a3-8c28-3251c6a8acccProduct name120140508
fe21f3fd-a378-0654-1972-db3c3b64470eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0037-6822-102024-01-30C16284748780-11030e365-2f12-111a-e063-dadaa90a10e23831e931-ec0a-11e3-ac10-0800200c9a66

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0037-6822-10PROCTOFOAMHC1 in 1 CARTONAEROSOL, FOAM110
0037-6822-10PROCTOFOAMHC10 g in 1 CANISTERAEROSOL, FOAM1010

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0037-6822-10GM - Gram0037-6822d07a3823-26ee-42fe-afb1-431cef27eb3712014-11-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HYDROCORTISONE ACETATEACTIVE INGREDIENT3X7931PO742
PRAMOXINE HYDROCHLORIDEACTIVE INGREDIENT88AYB867L52
HYDROCORTISONEACTIVE MOIETYWI4X0X7BPJ2
PRAMOXINEACTIVE MOIETY068X84E0562
CETYL ALCOHOLINACTIVE INGREDIENT936JST6JCN2
GLYCERYL MONOSTEARATEINACTIVE INGREDIENT230OU9XXE42
ISOBUTANEINACTIVE INGREDIENTBXR49TP6112
LAURETH-23INACTIVE INGREDIENTN72LMW566G2
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9T2
PEG-100 STEARATEINACTIVE INGREDIENTYD01N1999R2
POLYOXYL 40 STEARATEINACTIVE INGREDIENT13A4J4NH9I2
PROPANEINACTIVE INGREDIENTT75W9911L62
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V32
PROPYLPARABENINACTIVE INGREDIENTZ8IX2SC1OH2
TROLAMINEINACTIVE INGREDIENT9O3K93S3TK2
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0037-68220037-6822-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 24 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4AEROSOL, FOAM / TOPICAL3.27 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PROPYLPARABENPROPYLPARABENZ8IX2SC1OHAEROSOL, FOAM / TOPICAL0.04 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PROPYLENE GLYCOLPROPYLENE GLYCOL6DC9Q167V3AEROSOL, FOAM / TOPICAL1800 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ISOBUTANEISOBUTANEBXR49TP611AEROSOL, FOAM / TOPICAL18 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PEG-100 STEARATEPEG-100 MONOSTEARATEYD01N1999RCREAM / TOPICAL552 mgExact identifier — unii+route
4 equally ranked IID candidates
LAURETH-23LAURETH-23N72LMW566GAEROSOL, FOAM / TOPICAL1.08 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNAEROSOL, FOAM / TOPICAL82 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PEG-100 STEARATEPEG-100 MONOSTEARATEYD01N1999RCREAM / TOPICAL552 mgExact identifier — unii+route
4 equally ranked IID candidates
PROPANEPROPANET75W9911L6AEROSOL, FOAM / TOPICAL55 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PROPANEPROPANET75W9911L6AEROSOL, FOAM / TOPICAL55 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
POLYOXYL 40 STEARATEPOLYOXYL 40 STEARATE TYPE I13A4J4NH9IAEROSOL, FOAM / TOPICAL2.83 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
TROLAMINETROLAMINE9O3K93S3TKAEROSOL, FOAM / TOPICAL2.6 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PROPYLPARABENPROPYLPARABENZ8IX2SC1OHAEROSOL, FOAM / TOPICAL0.04 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PROPYLENE GLYCOLPROPYLENE GLYCOL6DC9Q167V3AEROSOL, FOAM / TOPICAL1800 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
TROLAMINETROLAMINE9O3K93S3TKAEROSOL, FOAM / TOPICAL2.6 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TAEROSOL, FOAM / TOPICAL0.16 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TAEROSOL, FOAM / TOPICAL0.16 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNAEROSOL, FOAM / TOPICAL82 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PEG-100 STEARATEPEG-100 MONOSTEARATEYD01N1999RLOTION / TOPICAL1 %w/wExact identifier — unii+route
4 equally ranked IID candidates
ISOBUTANEISOBUTANEBXR49TP611AEROSOL, FOAM / TOPICAL18 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PEG-100 STEARATEPEG-100 MONOSTEARATEYD01N1999RLOTION / TOPICAL1 %w/wExact identifier — unii+route
4 equally ranked IID candidates
POLYOXYL 40 STEARATEPOLYOXYL 40 STEARATE TYPE I13A4J4NH9IAEROSOL, FOAM / TOPICAL2.83 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4AEROSOL, FOAM / TOPICAL3.27 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
LAURETH-23LAURETH-23N72LMW566GAEROSOL, FOAM / TOPICAL1.08 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A086195-001PROCTOFOAM HCHYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 1 matching rows.

Application-product, TE code table
Application-productTE code
A086195-001BX

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 198284e616aacf4f…
2026-08-18 06:07:402026-07A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 198231067a03dcf5…
2025-08-23 18:47 UTC2025-08A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19826a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 198203ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19822680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19825bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 198279d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19821e350fbaab3a…
2024-05-31 18:47 UTC2024-05A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19828072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19825c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19825d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19824b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXApproved before 198274a2ff9319b5…
2022-03-09 01:35 UTC2022-03A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXApproved before 198287673890dc5c…
2021-03-12 10:30 UTC2021-03A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXApproved before 19825aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXApproved before 19828869cabd3fbd…
2020-11-12 02:37 UTC2020-11A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXApproved before 1982c0c555d07b60…
2019-12-14 00:12 UTC2019-12A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXApproved before 19823f01610625f2…
2019-09-15 20:21 UTC2019-09A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXApproved before 1982b00525d2431f…
2019-07-19 19:46 UTC2019-07A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXApproved before 1982ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19826a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19821c564ffb4f44…
2023-12-20 04:57 UTC2023-12A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19829b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19823f0d92c62455…
2023-05-13 08:27 UTC2023-05A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982053a50430f4f…
2023-01-26 05:58 UTC2023-01A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19823bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 19823a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A086195-001PROCTOFOAM HC1%;1%AEROSOL, METERED / TOPICALBXRLD, RS, Approved before 1982f41ea6bd6efb…

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-09-14 22:38:342026-08A086195-001BX184e616aacf4f…
2026-08-18 06:07:402026-07A086195-001BX1caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A086195-001BX1011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A086195-001BX131067a03dcf5…
2025-08-23 18:47 UTC2025-08A086195-001BX16a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A086195-001BX1fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A086195-001BX1b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A086195-001BX103ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A086195-001BX12680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A086195-001BX15bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A086195-001BX1d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A086195-001BX1d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A086195-001BX179d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A086195-001BX1301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A086195-001BX11e350fbaab3a…
2024-05-31 18:47 UTC2024-05A086195-001BX18072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A086195-001BX15c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A086195-001BX15d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A086195-001BX14b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A086195-001BX174a2ff9319b5…
2022-03-09 01:35 UTC2022-03A086195-001BX1bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A086195-001BX1782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A086195-001BX187673890dc5c…
2021-03-12 10:30 UTC2021-03A086195-001BX15aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A086195-001BX18869cabd3fbd…
2020-11-12 02:37 UTC2020-11A086195-001BX1c0c555d07b60…
2019-12-14 00:12 UTC2019-12A086195-001BX13f01610625f2…
2019-09-15 20:21 UTC2019-09A086195-001BX1b00525d2431f…
2019-07-19 19:46 UTC2019-07A086195-001BX1ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A086195-001BX16a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A086195-001BX11c564ffb4f44…
2023-12-20 04:57 UTC2023-12A086195-001BX1ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A086195-001BX1a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A086195-001BX19b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A086195-001BX1a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A086195-001BX13f0d92c62455…
2023-05-13 08:27 UTC2023-05A086195-001BX1053a50430f4f…
2023-01-26 05:58 UTC2023-01A086195-001BX13bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A086195-001BX13a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A086195-001BX1f41ea6bd6efb…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PROCTOFOAM HCPRAMOXINE HYDROCHLORIDE HYDROCORTISONE ACETATEViatris Specialty LLC3831e931-ec0a-11e3-ac10-0800200c9a662025-04-15Warnings, Adverse reactionsExact identifier
ndc (package): 0037-6822-10
ndc (product): 0037-6822
ndc11 (package): 00037682210
spl id: d63033a1-dca0-44f9-a6f3-210e38c2691e
spl set id: 3831e931-ec0a-11e3-ac10-0800200c9a66

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.