Preparation H
- Product NDC
- 0573-2884
- 11-digit product format
- 005732884
- Labeler code
- 0573
- Product ID
- 0573-2884_155865d1-91f7-90d4-e063-6394a90a5945
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- cocoa butter, phenylephrine hydrochloride, and witch hazel
- Dosage form
- KIT
- Labeler
- Haleon US Holdings LLC
- Application
- M015
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-07-01
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2022-08-30 03:57 UTC · source 2022-08-29 | excluded product | product | fb8cb913e6d1… | eb8c232b6be0… | |
| 2022-08-30 03:57 UTC · source 2022-08-29 | excluded package | package | 0573-2884-12 | fb8cb913e6d1… | eb8c232b6be0… |
| 2022-04-09 23:13 UTC · source 2022-04-08 | excluded product | product | 86f5da6cb304… | a595104c45d7… | |
| 2022-04-09 23:13 UTC · source 2022-04-08 | excluded package | package | 0573-2884-12 | 86f5da6cb304… | a595104c45d7… |
| 2022-04-04 05:40 UTC · source 2022-04-01 | excluded product | product | bd6a592717d7… | 303034d00443… | |
| 2022-04-04 05:40 UTC · source 2022-04-01 | excluded package | package | 0573-2884-12 | bd6a592717d7… | 303034d00443… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Preparation H
- Listing expiration
- 2026-12-31
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2f370875-0225-47b7-b43f-8fa4600d2a0e | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| e4e263da-1c53-440f-bb80-b7a575843b5a | Product name | 1 | 20260313 |
| d2168cac-a261-415a-9c78-3522859fa720 | Product name | 3 | 20251124 |
| 05a8cdd1-eeb8-409e-b938-0778225eca7d | Product name | 4 | 20250221 |
| e5b5c132-b15d-435b-9faa-2f74e5cadcf9 | Product name | 8 | 20250220 |
| f489e8f3-5c9e-4818-b539-a73587edcfc7 | Product name | 2 | 20240229 |
| 0f7ae452-206d-4fc4-868d-56fc47074084 | Product name | 1 | 20231011 |
| e2db08c6-133f-4f4f-afb4-e90a2418d6f6 | Product name | 1 | 20230320 |
| ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906 | Product name | 7 | 20210625 |
| f52be47f-7aa7-46c0-b1fa-50c18dd50206 | Product name | 1 | 20201029 |
| b5abe2e3-39a1-43eb-9bff-f3c1653fe3df | Product name | 2 | 20190930 |
| 11ed6f83-cdd2-4637-8379-b1a1d3ae3cde | Product name | 1 | 20181101 |
| 86c45a79-b9f0-4476-a27c-6e10db098497 | Product name | 1 | 20180125 |
| e0b6c8be-f2bd-9f86-a9fc-3ed56ffaa814 | Product name | 3 | 20150910 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| 42f3c020-f1b3-89bc-7bdc-e1f10e680485 | Product name | 1 | 20140508 |
| e949165d-714d-e548-2b76-0cb5def16f30 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0573-2884-12 | 2023-02-08 | C162847 | 48780-1 | d6a99b39-6597-a426-e053-dadaa90af4c2 | Drug Facts |
| 0573-2884-12 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-6597-a426-e053-dadaa90af4c2 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0573-2884-12 | Preparation H | 1 in 1 CARTON | KIT | 1 | 7 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| GoodSense Hemorrhoidal Pain Relief | GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HCL | Perrigo Direct, Inc | 2e5f699d-45e8-6451-e063-6394a90a8ad8 | 2025-07-20 | Warnings | M015 |
| Good Sense Hemorrhoidal | COCOA BUTTER, PHENYLEPHRINE HCL | L. Perrigo Company | 379f8738-a871-4b09-abd1-c86386dfee04 | 2025-07-15 | Warnings | M015 |
| Maximum Strength Hemorrhoidal Pads | WITCH HAZEL | Walmart, Inc. | 6dd8d3d9-5109-4869-917b-9521e9ba1ed0 | 2025-07-14 | Warnings | M015 |
| Nikzon Hemorrhoidal | GLYCERIN, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE, AND PRAMOXINE HYDROCHLORIDE | Genomma Lab USA | 8f9a9939-2c99-489f-b597-9a51ec2684f9 | 2025-07-14 | Warnings | M015 |
| ReVIVOL-XR | PHENYLEPHRINE HYDROCHLORIDE | Unipack LLC | 2950fe83-a2a4-4ed4-b645-69d6fd2381ae | 2025-07-13 | Warnings | M015 |
| medicated wipes | WITCH HAZEL | Meijer Distribution Inc. | ba0f3f9a-95d1-4d8a-86d1-2c25c945118c | 2025-07-11 | Warnings | M015 |
| hemorrhoidal pads | WITCH HAZEL | Meijer Distribution Inc. | 53e39d22-a89e-4f95-8c64-abeb50f72ce7 | 2025-07-11 | Warnings | M015 |
| INVIGOR OH | LIDOCAINE | Natureplex LLC | 7c7b536d-e41a-4017-9df9-982e2e9cfe4e | 2025-07-10 | Warnings | M015 |
| Maximum Strength Hemorrhoidal Cream with Aloe | GLYCERIN, PHENYLEPHINE HCI, PRAMOXINE HCI, PETROLATUM | Chain Drug Marketing Association | 396ea654-8be1-591a-e063-6294a90a11e2 | 2025-07-08 | Warnings | M015 |
| PREPARATION H SOOTHING RELIEF ANTI-ITCH | HYDROCORTISONE | Haleon US Holdings LLC | d6148d77-ef6f-4552-b5ba-43b429923f19 | 2025-07-07 | Warnings | M015 |
| Rectal Care Cream | RECTAL CARE CREAM | Allegiant Health | ce585082-ad39-4b6f-a756-0d9a81a13eb8 | 2025-07-07 | Warnings | M015 |
| Bisacodyl Laxative | BISACODYL LAXATIVE SUPPOSITORIES | Neilmed Pharmaceuticals Inc. | 35cb0386-a662-6893-e063-6294a90aa71a | 2025-07-03 | Warnings | M015 |
| Hemorrhoidal Cream | GLYCEROL, PHENYLEPHINE, PRAMOXINE, PETROLATUM | Trifecta Pharmaceuticals Usa Llc | 38cf4e43-280b-eb96-e063-6294a90a5949 | 2025-07-02 | Warnings | M015 |
| TN Dickinsons Medicated Cooling Foam Hemorrhoidal Relief | WITCH HAZEL | Dickinson Brands Inc. | deca8ae2-53a3-4c90-aa10-45354e2cdab8 | 2025-06-27 | Warnings | M015 |
| Glycerin Laxative | GLYCERIN LAXATIVE SUPPOSITORIES | Neilmed Pharmaceuticals Inc. | 35cc266a-196f-16ce-e063-6394a90a24af | 2025-06-20 | Warnings | M015 |
| Phenylephrine Hemorrhoidal | HEMORRHOIDAL SUPPOSITORIES | Neilmed Pharmaceuticals Inc. | 35ccb320-e902-3d1a-e063-6294a90a68d5 | 2025-06-20 | Warnings | M015 |
| ProCure Hemorrhoidal | MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL | Twin Med LLC | 37a4cc43-0d53-f1bf-e063-6394a90a2dc9 | 2025-06-15 | Warnings | M015 |
| Hemorrhoidal Pain Relief | HEMORRHOIDAL PAIN RELIEF OINTMENT | Neilmed Pharmaceuticals Inc. | 374d89b6-9305-9adf-e063-6394a90adb32 | 2025-06-11 | Warnings | M015 |
| Dermoplast Post Partum | BENZOCAINE | Advantice Health, LLC | 374dced3-6527-b458-e063-6394a90a911e | 2025-06-11 | Warnings | M015 |
| foster and thrive hemorrhoidal | COCOA BUTTER, PHENYLEPHRINE HCL | Strategic Sourcing Services LLC | fb3bc359-b06b-4995-aa68-0117a639dff2 | 2025-06-11 | Warnings | M015 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1438497 | cocoa butter 88.4 % / phenylephrine HCl 0.25 % Rectal Suppository | PSN | 2f370875-0225-47b7-b43f-8fa4600d2a0e | 7 |
| 844379 | witch hazel 50 % Medicated Pad | PSN | 2f370875-0225-47b7-b43f-8fa4600d2a0e | 7 |
| 1438497 | cocoa butter 0.884 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Suppository | SCD | 2f370875-0225-47b7-b43f-8fa4600d2a0e | 7 |
| 844379 | witch hazel 500 MG/ML Medicated Pad | SCD | 2f370875-0225-47b7-b43f-8fa4600d2a0e | 7 |
| 1438497 | cocoa butter 88.4 % / phenylephrine HCl 0.25 % Rectal Suppository | SY | 2f370875-0225-47b7-b43f-8fa4600d2a0e | 7 |
| 844379 | witch hazel 50 % Medicated Pad | SY | 2f370875-0225-47b7-b43f-8fa4600d2a0e | 7 |
| 844379 | witch hazel 50 % Medicated Wipes | SY | 2f370875-0225-47b7-b43f-8fa4600d2a0e | 7 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0573-2884-12 | 00573288412 | 1 KIT in 1 CARTON (0573-2884-12) * 12 SUPPOSITORY in 1 BLISTER PACK * 4 CLOTH in 1 APPLICATOR | 1 kit | 2015-07-01 | 0000-00-00 | No | No | Current |