Witch Hazel
- Product NDC
- 41520-822
- 11-digit product format
- 415200822
- Labeler code
- 41520
- Product ID
- 41520-822_55648c77-8f5a-b589-e063-6394a90af031
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Witch Hazel
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- ADUSA Distribution, LLC
- Application
- M015
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-03-24
- Substance
- WITCH HAZEL
- Active strength
- 860 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
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
- Witch Hazel
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| WITCH HAZEL | 860 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 101I4J0U34 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 200295 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| c50d0496-6f09-43c2-9383-3250885968c9 | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 41520-822-43 | Witch Hazel | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | 16 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| WITCH HAZEL | ACTIVE INGREDIENT | 101I4J0U34 | WITCH HAZEL LIQUID [FOODHOLD U.S.A., LLC] | 1 | |
| WITCH HAZEL | ACTIVE MOIETY | 101I4J0U34 | WITCH HAZEL LIQUID [FOODHOLD U.S.A., LLC] | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | WITCH HAZEL LIQUID [FOODHOLD U.S.A., LLC] | 1 |
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 |
|---|---|---|---|---|
| 200295 | witch hazel 86 % Topical Solution | PSN | c50d0496-6f09-43c2-9383-3250885968c9 | 16 |
| 200295 | witch hazel 860 MG/ML Topical Solution | SCD | c50d0496-6f09-43c2-9383-3250885968c9 | 16 |
| 200295 | witch hazel 86 % Topical Solution | SY | c50d0496-6f09-43c2-9383-3250885968c9 | 16 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41520-822-43 | 41520082243 | 473 mL in 1 BOTTLE, PLASTIC (41520-822-43) | 473 ml | 2015-03-24 | 0000-00-00 | No | No | Current |