Headache Relief
- Product NDC
- 63868-485
- 11-digit product format
- 638680485
- Labeler code
- 63868
- Product ID
- 63868-485_db6c7572-59e0-4734-bfd6-1117dad5dd1b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Aspirin and caffeine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CHAIN DRUG MARKETING ASSOCIATION INC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1992-11-17
- Marketing end
- 2027-03-31
- Substance
- ACETAMINOPHEN; ASPIRIN; CAFFEINE
- Active strength
- 250; 250; 65 mg/1; mg/1; mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Headache Relief
- Brand name suffix
- Extra Strength
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 250 mg/1 |
| ASPIRIN | 250 mg/1 |
| CAFFEINE | 65 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D, R16CO5Y76E, 3G6A5W338E |
| Rxcui | 308297 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63868-485-01 | Headache ReliefExtra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 30 |
| 63868-485-01 | Headache ReliefExtra Strength | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | | 30 |
| 63868-485-02 | Headache ReliefExtra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 30 |
| 63868-485-02 | Headache ReliefExtra Strength | 200 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 200 | | 30 |
| 63868-485-24 | Headache ReliefExtra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 30 |
| 63868-485-24 | Headache ReliefExtra Strength | 24 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 24 | | 30 |
| 63868-485-50 | Headache ReliefExtra Strength | 50 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 50 | | 30 |
| 63868-485-50 | Headache ReliefExtra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 30 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| ACETAMINOPHEN | ACTIVE INGREDIENT | 362O9ITL9D | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| ASPIRIN | ACTIVE INGREDIENT | R16CO5Y76E | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| CAFFEINE | ACTIVE INGREDIENT | 3G6A5W338E | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| ACETAMINOPHEN | ACTIVE MOIETY | 362O9ITL9D | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| ASPIRIN | ACTIVE MOIETY | R16CO5Y76E | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| CAFFEINE | ACTIVE MOIETY | 3G6A5W338E | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| PROPYLENE GLYCOL | INACTIVE INGREDIENT | 6DC9Q167V3 | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 13 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63868-485 | HEADACHE RELIEF EXTRA STRENGTH (ACETAMINOPHEN, ASPIRIN AND CAFFEINE) TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC] | 29 | Current NDC, Legacy NDC, 8 package rows | 20240709_4005f8dd-3050-4590-8703-6997444e8df3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63868-485-01 | 63868048501 | 1 BOTTLE, PLASTIC in 1 CARTON (63868-485-01) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 1992-11-17 | 2027-03-31 | No | No | Current |
| 63868-485-02 | 63868048502 | 1 in 1 CARTON | | | | | Historical |
| 63868-485-24 | 63868048524 | 1 BOTTLE, PLASTIC in 1 CARTON (63868-485-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 1992-11-17 | 2027-03-31 | No | No | Current |
| 63868-485-50 | 63868048550 | 1 BOTTLE, PLASTIC in 1 CARTON (63868-485-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 1992-11-17 | 2027-03-31 | No | No | Current |