Indications and uses
For temporary relief of pain and itching due to minor skin irritations.
FranklyNumb 1
- Manufacturer
- Sambria Pharmaceuticals, LLC
- Effective date
- 2021-12-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:45:33
Label at a glance#
ProductFranklyNumb 1
Active ingredientBENZOCAINE
Label structure10 sections
Dosage and administration
For adults and children two-years or older: Apply to affected area not more than 3 or 4 times daily. Children under 2 years of age: consult a physician. Apply in a circular motion for 30 to 60 seconds.
Label contents#
Full prescribing information#
Active ingredient
Benzocaine 20%
Purpose
External Analgesic
Uses
For temporary relief of pain and itching due to minor skin irritations.
warnings
For external use only.
Avoid contact with eyes.
Do not use in large quantities, particularly over the raw surfaces or blistered area
Stop use and ask a doctor if
condition worsens, or if symptoms persists for more than 7 days or clear up and occur again within the few days. Discontinue use.
Keep out of reach of children
If product is swallowed, get medical help or contact a Poison Control Center right away
Directions
For adults and children two-years or older: Apply to affected area not more than 3 or 4 times
daily. Children under 2 years of age: consult a physician. Apply in a circular motion for 30 to 60 seconds.
Inactive ingredients
Aqua (Deionized Water), Arnica Montana Flower Extract, C13-14 Isoparaffin, Chrondroitin Sulfate,
Emu Oil, Ethoxydiglycol, Ethylhexyglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7,
Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmethane (MSM), Phenoxyethanol,Polyacrylamide,
Propylene Glycol,StearicAcid,Triethanolamine.
Other information
Protect this product from excessive heat and direct sun.
Questions or comments?
support@franklynumb.com
Product label
DailyMed RxNorm Mappings#
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| BENZOCAINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 54723-003-01 | 2023-01-30 | C162847 | 48780-1 | f386c649-b675-0266-e053-dadaa90a7c1a | f435c3ed-f99b-4baf-af07-69780cd3ef9b |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54723-003-01 | FranklyNumb 1 | 4 mL in 1 POUCH | CREAM | 4 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- FranklyNumb 1
- Benzocaine
- WATER
- ARNICA MONTANA FLOWER
- C13-14 ISOPARAFFIN
- CHONDROITIN SULFATE (BOVINE)
- EMU OIL
- DIETHYLENE GLYCOL MONOETHYL ETHER
- ETHYLHEXYLGLYCERIN
- GLUCOSAMINE SULFATE
- ISOPROPYL PALMITATE
- LAURETH-7
- TEA TREE OIL
- DIMETHYL SULFONE
- PHENOXYETHANOL
- POLYACRYLAMIDE (10000 MW)
- PROPYLENE GLYCOL
- STEARIC ACID
- TROLAMINE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 54723-003 | 54723-003-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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 |
|---|---|---|---|---|---|---|
| d2a9b04b-c9e8-5cde-e053-2995a90a4e07 | f435c3ed-f99b-4baf-af07-69780cd3ef9b | 2021-12-08 | Warnings | d2a9b04b-c9e8-5cde-e053-2995a90a4e07 f435c3ed-f99b-4baf-af07-69780cd3ef9b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.