Witch Hazel
- Product NDC
- 70677-1252
- 11-digit product format
- 706771252
- Labeler code
- 70677
- Product ID
- 70677-1252_d1cb4ea8-7b39-4145-9fbf-893d7f9a6f5d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Witch hazel
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-10-01
- Substance
- WITCH HAZEL
- Active strength
- 842 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 | 842 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 101I4J0U34 | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| ef3408db-de98-4a43-9215-f80fed14815c | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70677-1252-1 | Witch Hazel | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | 3 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70677-1252-1 | ML - Milliliter | 70677-1252 | bf1b0868-218c-4125-90b1-e2bb649cf8b0 | 1 | 2024-03-12 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70677-1252 | WITCH HAZEL LIQUID [STRATEGIC SOURCING SERVICES LLC] | 3 | Current NDC, 1 package rows | 20250416_ef3408db-de98-4a43-9215-f80fed14815c.zip |
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 |
|---|---|---|---|---|---|---|
| Anubis Barcelona New Even | LACTIC ACID, CITRIC ACID, GLYCOLIC ACID | ANUBIS COSMETICS SL | eaeeb6e0-5322-20c4-e053-2995a90a9fd9 | 2023-09-01 | Warnings | M016 |
| Anubis Barcelona Vital Line | HYDROLYZED COLLAGEN | ANUBIS COSMETICS SL | f564bbf0-3b5c-4a81-e053-2a95a90a7ea6 | 2023-08-29 | Warnings | M016 |
| Carmex Classic Lip Balm Medicated Free Cupcake Batter Stick Sunscreen SPF 15 | CAMPHOR (SYNTHETIC), PETROLATUM | Carma Laboratories, Inc. | 5378d653-702d-405c-a067-882554aaf93a | 2023-08-21 | Warnings | M016 |
| Quality Choice Anti-itch Medicated | CALAMINE AND PRAMOXINE HYDROCHLORIDE | CHAIN DRUG MARKETING ASSOCIATION INC | 5e07f26f-cfb6-57f9-e053-2991aa0a2008 | 2023-08-02 | Warnings | M016 |
| Barrier Balm | BARRIER BALM | Autumn Harp, Inc. | 01df9746-991b-4363-e063-6294a90aaac6 | 2023-08-01 | Warnings | M016 |
| Barrier Cream | ZINC OXIDE | Avasol LLC | bc6a2736-faa6-46d3-af9b-a70f0762e9ce | 2023-05-15 | Warnings | M016 |
| First Aid Beauty FAB Ultra Repair Skin Protectant Candy Cane | COLLOIDAL OATMEAL | The Procter & Gamble Manufacturing Company | bec2f702-5ff5-ea66-e053-2a95a90ad1ec | 2023-01-01 | Warnings | M016 |
| Badger After-BUG Balm | COLLOIDAL OATMEAL | W.S. Badger Company, Inc. | a623da47-cef2-146f-e053-2a95a90afe3a | 2021-11-17 | Warnings | M016 |
| Derma-e Eczema Relief | OATMEAL | Topiderm, Inc | e1797f81-af4b-49e1-9906-dbfd904a282b | 2020-08-19 | Warnings | M016 |
| Resurfix Plus | PETROLATUM | Topiderm, Inc. | f100f43d-6ace-4c3a-9c85-640c0ab2e360 | 2019-11-19 | Warnings | M016 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 70677-1252-1 | 70677125201 | 473 mL in 1 BOTTLE, PLASTIC (70677-1252-1) | 473 ml | 2023-10-01 | No | No | Current |