FIRST SHIELD
- Product NDC
- 72976-008
- 11-digit product format
- 729760008
- Labeler code
- 72976
- Product ID
- 72976-008_0eff7672-ef8d-8a09-e063-6394a90a62e9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride, Lidocaine HCI
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Ever Ready First Aid
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-11-23
- Substance
- LIDOCAINE HYDROCHLORIDE; BENZALKONIUM CHLORIDE
- Active strength
- 5; 1.3 mg/g; mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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
- FIRST SHIELD
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| LIDOCAINE HYDROCHLORIDE | 5 mg/g |
| BENZALKONIUM CHLORIDE | 1.3 mg/g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| V13007Z41A | Internal UNII lookup |
| F5UM2KM3W7 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1012100 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| ee198aa1-ad0d-9185-e053-2a95a90a6595 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 860a93dc-4863-49cc-b284-6bbe8191bc48 | Product name | 4 | 20250214 |
| eaba870a-6a9d-442e-8643-87b3f558a451 | Product name | 1 | 20250117 |
| 9b4cf230-fd05-41d5-98c6-5db9ecb27b86 | Product name | 1 | 20230117 |
| fa8b5901-e681-426f-82fe-54f6d81ec698 | Product name | 4 | 20180619 |
| 332d03e4-aa24-4b11-841a-02bf41081920 | Product name | 1 | 20171221 |
| c08ab52f-2fc8-4409-9d9f-ed8edc0bd070 | Product name | 1 | 20171221 |
| 68ed98f8-24c2-44a0-944a-6d36e82ce25a | Product name | 1 | 20141222 |
| 1cd42bc2-a430-c72b-636d-991b235fbf80 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72976-008-01 | FIRST SHIELD | 0.9 g in 1 POUCH | CREAM | 0.9 | 2 |
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 |
|---|---|---|---|---|---|---|
| Anti-Fungal Powder | MICONAZOLE NITRATE | TopCo Associates | 19c3fbc5-abde-57df-e063-6394a90a125c | 2025-11-06 | Warnings | M005 |
| Tolnaftate | FOOT ODOR CONTROL SPRAY | Topco Associates LLC | 17993a9f-0d44-43a1-8608-94ee8a08b539 | 2025-11-06 | Warnings | M005 |
| DVO Estriol cream | ESTRIOL0.2% | Guangzhou Huixue Biotechnology Co., Ltd. | 42e4cc84-7c00-6937-e063-6294a90a0c09 | 2025-11-05 | Warnings | M005 |
| Medline | MICONAZOL NITRATE | Medline Industries, LP | dad58efb-cc20-577a-e053-2a95a90abd9d | 2025-11-03 | Warnings | M005 |
| Tolnafate | TOLNAFTATE POWDER SPRAY | HEB | c6af941a-0b85-4611-a6f3-b13fcf3c4a87 | 2025-11-03 | Warnings | M005 |
| Tolnaftate | FOOT ODOR CONTROL SPRAY | HEB | c585605b-ecb8-4dd8-9205-a9be02d751fa | 2025-11-03 | Warnings | M005 |
| Premier Solutions Antifungal Tolnaftate Liquid | TOLNAFTATE | Premier Brands of America, Inc. | e1971c1c-5687-577b-e053-2a95a90ad95f | 2025-11-03 | Warnings | M005 |
| Miconazole nitrate | ANTIFUNGAL MICONAZOLE LIQUID CONTINUOUS SPRAY | Premier Brands of America Inc. | 3803c643-35d1-06d4-e063-6294a90ac6f6 | 2025-11-03 | Warnings | M005 |
| Anti-fungal Powder Miconazole Nitrate | MICONAZOLE NITRATE | Meijer Distribution Inc | 03fd069d-685d-b8ac-e063-6394a90a31f8 | 2025-10-31 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | Premier Brands of America Inc. | 7a6a63cd-e87d-4229-8acf-b65d63909eb6 | 2025-10-31 | Warnings | M005 |
| Azolen | MICONAZOLE NITRATE | Stratus Pharmaceuticals, Inc. | 9c2574f3-3be4-405a-9c87-943dc6ef8777 | 2025-10-30 | Warnings | M005 |
| Family Care Antifungal | CLOTRIMAZOLE | United Exchange Corp. | 63255079-ecf1-1e77-e053-2a91aa0a7b6c | 2025-10-30 | Warnings | M005 |
| Miconazorb AF | MICONAZOLE NITRATE | AmerisourceBergen Drug Corporation | 13a20d21-42d5-fe56-e063-6394a90aaf57 | 2025-10-30 | Warnings | M005 |
| Antifungal Liquid Continuous | MICONAZOLE NITRATE | Family Dollar Services, Inc | 17cc4601-f946-df8b-e063-6394a90a3897 | 2025-10-30 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | ARMY & AIR FORCE EXCHANGE SERVICE | 932b1be8-3dbb-49ae-822a-c44a24fbe36a | 2025-10-30 | Warnings | M005 |
| Miconazole nitrate | ANTIFUNGAL MICONAZOLE LIQUID CONTINUOUS SPRAY | GEISS, DESTIN AND DUNN, INC. | c367c2e8-5423-bf01-e053-2a95a90ab8e9 | 2025-10-30 | Warnings | M005 |
| Miconazole Nitrate | JOCK ITCH SPRAY | Harris Teeter, LLC | 636b0d6f-4e36-4c96-9e71-7bfdebb7f3cb | 2025-10-30 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | Harris Teeter, LLC | f140e9bb-507b-4048-8b7b-8cc51b6a497d | 2025-10-30 | Warnings | M005 |
| HEB Athlete Foot Antifungal | MICONAZOLE NITRATE | HEB | 2e204111-b5d3-0220-e063-6294a90a67bb | 2025-10-30 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL SPRAY LIQUID | Kroger Co. | 0cfebac3-684d-4599-b75f-9a82708db717 | 2025-10-30 | Warnings | M005 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1012100 | benzalkonium chloride 0.13 % / lidocaine HCl 0.5 % Topical Cream | PSN | ee198aa1-ad0d-9185-e053-2a95a90a6595 | 2 |
| 1012100 | benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 5 MG/ML Topical Cream | SCD | ee198aa1-ad0d-9185-e053-2a95a90a6595 | 2 |
| 1012100 | benzalkonium chloride 0.13 % / lidocaine hydrochloride 0.5 % Topical Cream | SY | ee198aa1-ad0d-9185-e053-2a95a90a6595 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 72976-008-01 | 72976000801 | .9 g in 1 POUCH (72976-008-01) | 2022-11-23 | 0000-00-00 | No | No | Current |