Hand Recovery
- Product NDC
- 70741-007
- Requested package NDC
- 70741-007-01
- 11-digit product format
- 707410007
- Labeler code
- 70741
- Product ID
- 70741-007_21e8c2a4-36a7-40db-9681-244bcef7e8a4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Derma Glove
- Application
- part333A
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-01-06
- Substance
- ALCOHOL
- Active strength
- 70 mL/100mL
- 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 | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2022-08-30 03:57 UTC · source 2022-08-29 | excluded package | package | 70741-007 | 70741-007-01 | I | Inactivated by FDA | excluded / ndc_excluded.zip | fb8cb913e6d1… | eb8c232b6be0… | |
| 2022-04-09 23:13 UTC · source 2022-04-08 | excluded package | package | 70741-007 | 70741-007-01 | I | Inactivated by FDA | excluded / ndc_excluded.zip | 86f5da6cb304… | a595104c45d7… | |
| 2022-04-04 05:40 UTC · source 2022-04-01 | excluded package | package | 70741-007 | 70741-007-01 | I | Inactivated by FDA | excluded / ndc_excluded.zip | bd6a592717d7… | 303034d00443… |
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hand Recovery
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ALCOHOL | 70 mL/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 3K9958V90M | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1809903 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 074a760f-9031-40c1-9867-95ef0345418d | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 7792dadb-52b6-46b6-8fdf-80b1171065b5 | Product name | 1 | 20180810 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70741-007-04 | Hand Recovery | 236.8 mL in 1 PACKAGE | Lotion | 236.8 | 9 | |
| 70741-007-01 | Hand Recovery | 25 mL in 1 PACKAGE | Lotion | 25 | 7 | |
| 70741-007-02 | Hand Recovery | 40 mL in 1 PACKAGE | Lotion | 40 | 7 | |
| 70741-007-03 | Hand Recovery | 75 mL in 1 PACKAGE | Lotion | 75 | 6 | |
| 70741-007-05 | Hand Recovery | 473.6 mL in 1 PACKAGE | Lotion | 473.6 | 6 | |
| 70741-007-06 | Hand Recovery | 947.2 mL in 1 PACKAGE | Lotion | 947.2 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70741-007 | HAND RECOVERY (ALCOHOL) LOTION [DERMA GLOVE] | 7 | Current NDC, Legacy NDC, 1 package rows | 20241011_e6cfe092-cb2c-441b-8897-98626c43bef8.zip |
| 70741-007 | HAND RECOVERY (ALCOHOL) LOTION [DERMA GLOVE] | 7 | Current NDC, Legacy NDC, 1 package rows | 20241011_b4ff67d6-27d6-4d31-a708-9c2e8d4f0f3e.zip |
| 70741-007 | HAND RECOVERY (ALCOHOL) LOTION [DERMA GLOVE] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241011_d8705086-7209-4f13-bd54-604c90495f0a.zip |
| 70741-007 | HAND RECOVERY (ALCOHOL) LOTION [DERMA GLOVE] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250110_074a760f-9031-40c1-9867-95ef0345418d.zip |
| 70741-007 | HAND RECOVERY (ALCOHOL) LOTION [DERMA GLOVE] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241011_06f74478-57aa-4b8d-b888-55e1ee4fbd45.zip |
| 70741-007 | HAND RECOVERY (ALCOHOL) LOTION [DERMA GLOVE] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241011_90058ba8-e55d-4318-9fc5-8f0d25dfdd99.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 |
|---|---|---|---|---|---|---|
| Hand Recovery | ALCOHOL | Derma Glove | 90058ba8-e55d-4318-9fc5-8f0d25dfdd99 | 2025-11-14 | Warnings | 70741-007 |
| Hand Recovery | ALCOHOL | Derma Glove | 074a760f-9031-40c1-9867-95ef0345418d | 2025-01-08 | Warnings | 70741-007 |
| Hand Recovery | ALCOHOL | Derma Glove | 06f74478-57aa-4b8d-b888-55e1ee4fbd45 | 2024-10-09 | Warnings | 70741-007 |
| Hand Recovery | ALCOHOL | Derma Glove | e6cfe092-cb2c-441b-8897-98626c43bef8 | 2024-10-09 | Warnings | 70741-007 |
| Hand Recovery | ALCOHOL | Derma Glove | b4ff67d6-27d6-4d31-a708-9c2e8d4f0f3e | 2024-10-09 | Warnings | 70741-007-01 70741-007 70741000701 |
| Hand Recovery | ALCOHOL | Derma Glove | d8705086-7209-4f13-bd54-604c90495f0a | 2024-10-09 | Warnings | 70741-007 |
DailyMed RxNorm Mappings#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70741-007-01 | 70741000701 | 25 mL in 1 PACKAGE (70741-007-01) | 25 ml | 2017-01-06 | 0000-00-00 | No | No | Current |