Tension Headache Relief
- Manufacturer
- Hi-Tech Nutraceuticals, LLC
- Effective date
- 2026-03-31
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 01:52:22
Label at a glance#
ProductTension Headache Relief
Active ingredientACETAMINOPHEN, CAFFEINE
Label structure17 sections
Label contents#
Full prescribing information#
OTC - ASK DOCTOR SECTION
OTC - ASK DOCTOR/PHARMACIST SECTION
OTC - DO NOT USE SECTION
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
OTC - PREGNANCY OR BREAST FEEDING SECTION
OTC - PURPOSE SECTION
OTC - QUESTIONS SECTION
OTC - STOP USE SECTION
OTC - WHEN USING SECTION
DOSAGE & ADMINISTRATION SECTION
WARNINGS SECTION
INACTIVE INGREDIENT SECTION
STORAGE AND HANDLING SECTION
OVERDOSAGE SECTION
INDICATIONS & USAGE SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| CAFFEINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 7dea7767-9f52-b60a-5435-33cb9cc28bae | Product name | 4 | 20250124 |
| 6338270f-96cb-0ecb-6fbb-0a9bc78001f4 | Product name | 7 | 20250116 |
| 0ca83774-3f79-b837-5d6f-c210102f3bc8 | Product name | 6 | 20250114 |
| 41b814f3-0166-1c53-c9ef-a0794c7daf9d | Product name | 3 | 20221110 |
| a590be26-846c-8659-a5a1-fb25907965dc | Product name | 2 | 20221110 |
| 2dc76302-91c0-4c35-ad78-99adfb049c4b | Product name | 1 | 20200603 |
| e6065d4b-5ae1-476f-a40e-f2851cbb5d2b | Product name | 2 | 20180221 |
| f212291f-05fe-9603-fc7e-bd73e38ce1e6 | Product name | 2 | 20161129 |
| 182f9ab4-4ab5-c449-200f-87ce2ce8e550 | Product name | 2 | 20151105 |
| 332e86c3-7875-ca6e-f934-2206d2b31996 | Product name | 1 | 20140508 |
| 56625fcc-aa34-9d30-d0e9-1c1beb37ea21 | Product name | 1 | 20140508 |
| 7dfac40f-a405-cd2e-7c06-3059ec0e1092 | Product name | 1 | 20140508 |
| 96c2be53-8e44-452d-56a2-d255b2f1af2d | Product name | 1 | 20140508 |
| bf8bd5f7-495f-4022-2780-7ded7ea7ea44 | Product name | 1 | 20140508 |
| d223c173-c39b-d764-47d4-d671d3088815 | Product name | 1 | 20140508 |
| e01133ad-4dcd-c7f3-454b-2ff569ee160a | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69732-007-01 | 2024-01-30 | C162847 | 48780-1 | 1030e365-51dd-111a-e063-dadaa90a10e2 | b119ba37-0ee3-851a-e053-2995a90a85b1 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69732-007-01 | Tension Headache Relief | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | 4 |
Products#
Every source-derived product name is available through these pages.
- Tension Headache Relief
- Acetaminophen, Caffeine
- ACETAMINOPHEN
- SILICON DIOXIDE
- MICROCRYSTALLINE CELLULOSE
- MAGNESIUM STEARATE
- SODIUM STARCH GLYCOLATE TYPE A
- CAFFEINE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69732-007 | 69732-007-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| SODIUM STARCH GLYCOLATE TYPE A | H8AV0SQX4D | IACT |
| CAFFEINE | 3G6A5W338E | ACTIB |
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 |
|---|---|---|---|---|---|---|
| Tension Headache Relief | ACETAMINOPHEN, CAFFEINE | Hi-Tech Nutraceuticals, LLC | b119ba37-0ee3-851a-e053-2995a90a85b1 | 2026-03-31 | Warnings | 69732-007-01 69732-007 69732000701 4e542499-5955-50a8-e063-6294a90a46ed b119ba37-0ee3-851a-e053-2995a90a85b1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.















