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 |
|---|---|---|---|---|---|---|
| Medline | MENTHOL, WHITE PETROLATUM, ZINC OXIDE | Medline Industries, LP | 006539c9-1982-d6de-e063-6294a90a1a5a | 2025-10-17 | Warnings | M015 |
| Xesso Strawberry Rear Comfort Glide 4% Lidocaine | LIDOCAINE | Premium Natural Cosmetics Inc | efba09fc-6dd7-0f73-e053-2995a90a628a | 2025-10-17 | Warnings | M015 |
| medicated pads | WITCH HAZEL | TARGET CORPORATION | acd0d99d-2a77-4227-bebb-c819f4a52666 | 2025-10-14 | Warnings | M015 |
| Acolye Numbing Cream Anorectal(Hemorrhoidal) Cream | LIDOCAINE | Guangzhou Haishi Biological Technology Co., Ltd. | 40b0e8d6-4686-960b-e063-6294a90a016e | 2025-10-09 | Warnings | M015 |
| Acolye Numbing Cream Anorectal(Hemorrhoidal) Cream | LIDOCAINE | Guangzhou Haishi Biological Technology Co., Ltd. | 40b452a3-76b7-2433-e063-6294a90ab6b4 | 2025-10-09 | Warnings | M015 |
| EQUATE HEMORRHOID RELIEF | LIDOCAIN 5% | WALMART, INC | d96e8152-e36e-22fc-e053-2995a90a8b2b | 2025-10-08 | Warnings | M015 |
| Pramoxine Hydrochloride Anorectal | PRAMOXINE HYDROCHLORIDE | Stratus Pharmaceuticals | 39a16b66-b0e9-412f-8773-8dec0a1227e0 | 2025-10-02 | Warnings | M015 |
| Doctor Butlers Hemorrhoid and Fissure External Pain Formula | LIDOCAINE 5% | Beyond Health, P.A. | d92f22a7-c0b5-d8b8-e053-2a95a90a2376 | 2025-09-30 | Warnings | M015 |
| RWWXII Deep Numbing Cream(Anorectal Hemorrhoidal Cream) | LIDOCAINE | Guangzhou Haishi Biological Technology Co., Ltd. | 3ffc57c7-5bf4-cba8-e063-6394a90a322f | 2025-09-29 | Warnings | M015 |
| Hemorrhoidal Pain Relief | HEMORRHOIDAL PAIN RELIEF CREAM | Neilmed Pharmaceuticals Inc. | 374dc1c0-4243-b272-e063-6394a90a5a6b | 2025-09-24 | Warnings | M015 |
| Medi-First Burn | LIDOCAINE HYDROCHLORIDE | Unifirst First Aid Corporation | 44bb5f25-1114-4bb1-8bcf-40402594abc4 | 2025-09-09 | Warnings | M015 |
| Dr. Care Numbing Cream | 5% LIDOCAINE | Shengnan (Guangzhou) Cosmetics Co., LTD | 3e456af7-9726-d17e-e063-6394a90ab560 | 2025-09-08 | Warnings | M015 |
| Medi-first Ivy-Rid First Aid | BENZOCAINE AND BENZETHONIUM CHLORIDE | Unifirst First Aid Corporation | 905c97ad-0bba-46b1-939c-f16fbdb02818 | 2025-09-08 | Warnings | M015 |
| MediFirst Burn | LIDOCAINE HYDROCHLORIDE | Unifirst First Aid Corporation | 9fa5b348-29c2-4cd0-a945-0486bd27f5e0 | 2025-09-08 | Warnings | M015 |
| Medi-First Burn | LIDOCAINE HCL | Unifirst First Aid Corporation | b3ebf104-cc51-0ef5-e053-2a95a90a25c9 | 2025-09-08 | Warnings | M015 |
| Lidocaine Hydrochloride | LIDOCAINE HYDROCHLORIDE | Unifirst First Aid Corporation | 4c2e2b91-d2f6-4e41-9a4c-ecabca9830e8 | 2025-09-08 | Warnings | M015 |
| Pain Relief | ANALGESIC MENTHOL | Unifirst First Aid Corporation | 8162d22d-04c0-de07-e053-2991aa0a9975 | 2025-09-08 | Warnings | M015 |
| Green Guard Burn | LIDOCAINE HCL | Unifirst First Aid Corporation | b451e96f-fcba-6495-e053-2a95a90a2adf | 2025-09-08 | Warnings | M015 |
| Lidochill(TM) Gel | LIDOCAINE HCL 4%, MENTHOL 1% | PureTek Corporation | d2a9aeb6-8a94-49e7-ab46-84403560b6c8 | 2025-09-08 | Warnings | M015 |
| Signature numbing cream | 5% LIDOCAINE | Shengnan (Guangzhou) Cosmetics Co., LTD | 3e1892de-378b-d2d0-e063-6294a90ad7db | 2025-09-05 | 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 |