Xlear Max
- Manufacturer
- Xlear Inc
- Effective date
- 2016-07-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:08:08
Label at a glance#
ProductXlear Max
Active ingredientCAPSICUM ANNUUM WHOLE
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 27017-019-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-d003-f424-e053-dadaa90a57ce | 0e961ac2-50d9-4772-8330-c3ef6057bc50 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 27017-019-01 | Xlear Max | 45 g in 1 BOTTLE, SPRAY | SPRAY, METERED | 45 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Xlear Max
- homeopathic nasal spray
- CAPSICUM ANNUUM WHOLE
- ALOE VERA WHOLE
- SODIUM CHLORIDE
- GRAPEFRUIT SEED OIL
- WATER
- XYLITOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 27017-019 | 27017-019-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CAPSICUM ANNUUM WHOLE | 7FKZ3QQQ1F | ACTIB |
| ALOE VERA WHOLE | KIZ4X2EHYX | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| GRAPEFRUIT SEED OIL | 598D944HOL | IACT |
| WATER | 059QF0KO0R | IACT |
| XYLITOL | VCQ006KQ1E | IACT |
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 |
|---|---|---|---|---|---|---|
| 0d544bcc-babe-40eb-8c51-e5e40142fae9 | 0e961ac2-50d9-4772-8330-c3ef6057bc50 | 2016-07-13 | 0d544bcc-babe-40eb-8c51-e5e40142fae9 0e961ac2-50d9-4772-8330-c3ef6057bc50 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

