NDC 0135-0607
Panadol Cold and Flu NonDrowsy
Acetaminophen And Phenyleprine Hcl
Panadol Cold and Flu NonDrowsy is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Acetaminophen; Phenylephrine Hydrochloride.
| Product ID | 0135-0607_08c94755-c510-4e14-a0df-6672fcbfccf0 |
| NDC | 0135-0607 |
| Product Type | Human Otc Drug |
| Proprietary Name | Panadol Cold and Flu NonDrowsy |
| Generic Name | Acetaminophen And Phenyleprine Hcl |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2017-06-01 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| Substance Name | ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient Strength | 325 mg/1; mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
Packaging
NDC 0135-0607-02
3 BLISTER PACK in 1 CARTON (0135-0607-02) > 8 TABLET, FILM COATED in 1 BLISTER PACK
| Marketing Start Date | 2017-06-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 0135-0607-01 [00135060701]
Panadol Cold and Flu NonDrowsy TABLET, FILM COATED
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-06-01 |
NDC 0135-0607-03 [00135060703]
Panadol Cold and Flu NonDrowsy TABLET, FILM COATED
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-06-01 |
NDC 0135-0607-02 [00135060702]
Panadol Cold and Flu NonDrowsy TABLET, FILM COATED
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-06-01 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 325 mg/1 |
OpenFDA Data
| SPL SET ID: | f626ab17-01c9-4493-ba9e-0c8c11146384 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
NDC Crossover Matching brand name "Panadol Cold and Flu NonDrowsy" or generic name "Acetaminophen And Phenyleprine Hcl"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0135-0607 | Panadol | acetaminophen and phenyleprine HCl |
| 0135-7031 | Panadol | acetaminophen and phenyleprine HCl |
Trademark Results [Panadol]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PANADOL 98688417 not registered Live/Pending |
Haleon UK IP Limited 2024-08-08 |
 PANADOL 98675464 not registered Live/Pending |
Haleon UK IP Limited 2024-07-31 |
 PANADOL 87707023 5512890 Live/Registered |
GlaxoSmithKline Consumer Healthcare (UK) IP Limited 2017-12-04 |
 PANADOL 85678959 4408281 Live/Registered |
GLAXOSMITHKLINE CONSUMER HEALTHCARE (UK) IP LIMITED 2012-07-17 |
 PANADOL 73094226 1060597 Live/Registered |
STERLING DRUG INC. 1976-07-22 |
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