NDC 49738-484

Smart Sense pain relief extra strength

Acetaminophen

Smart Sense pain relief extra strength is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Kmart Corporation. The primary component is Acetaminophen.

• Product ID: 49738-484_1ad96536-cd26-4b96-9081-f640ca523b73
• NDC: 49738-484
• Product Type: Human Otc Drug
• Proprietary Name: Smart Sense pain relief extra strength
• Generic Name: Acetaminophen
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2010-05-20
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: Kmart Corporation
• Substance Name: ACETAMINOPHEN
• Active Ingredient Strength: 500 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 49738-484-78

1 BOTTLE in 1 CARTON (49738-484-78) > 100 TABLET in 1 BOTTLE

• Marketing Start Date: 2010-05-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 49738-484-78 [49738048478]

Smart Sense pain relief extra strength TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-05-20

NDC 49738-484-82 [49738048482]

Smart Sense pain relief extra strength TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-05-20

NDC 49738-484-62 [49738048462]

Smart Sense pain relief extra strength TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-05-20

NDC 49738-484-71 [49738048471]

Smart Sense pain relief extra strength TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-05-20

NDC 49738-484-90 [49738048490]

Smart Sense pain relief extra strength TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-05-20

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	500 mg/1

OpenFDA Data

• SPL SET ID: fa64379b-f541-41db-9dd2-499e290b3f5d
• Manufacturer:
  • Kmart Corporation
• UNII:
  • 362O9ITL9D
• RxNorm Concept Unique ID - RxCUI:
  • 198440
• UPC Code:
  • 0883967395026

NDC Crossover Matching brand name "Smart Sense pain relief extra strength" or generic name "Acetaminophen"

NDC	Brand Name	Generic Name
49738-484	Smart Sense pain relief extra strength	Smart Sense pain relief extra strength
49738-227	Smart Sense pain relief extra strength	Smart Sense pain relief extra strength
0121-0657	Acetaminophen	Acetaminophen
0113-7000	Basic Care acetaminophen	Acetaminophen
0113-7484	basic care acetaminophen	Acetaminophen
0113-7544	Basic Care Acetaminophen	Acetaminophen
0113-7130	basic care childrens pain and fever	Acetaminophen
0113-0020	good sense childrens pain and fever	Acetaminophen
0113-0212	Good Sense Childrens Pain and Fever	Acetaminophen
0113-0608	good sense childrens pain and fever	Acetaminophen
0113-0998	Good Sense Childrens Pain and Fever	Acetaminophen
0113-0161	Good Sense pain and fever	Acetaminophen
0113-0397	Good Sense Pain and Fever	acetaminophen
0113-0590	Good Sense Pain and Fever	acetaminophen
0113-0946	good sense pain and fever	Acetaminophen
0113-8959	Good Sense Pain and Fever	Acetaminophen
0113-0025	Good Sense Pain Relief	Acetaminophen
0113-0044	Good Sense Pain Relief	Acetaminophen
0113-0187	good sense pain relief	Acetaminophen
0113-0217	good sense pain relief	Acetaminophen
0113-0227	Good Sense Pain Relief	Acetaminophen
0113-0403	good sense pain relief	Acetaminophen
0113-0484	Good Sense Pain Relief	Acetaminophen
0113-0518	good sense pain relief	Acetaminophen
0113-0544	good sense pain relief	Acetaminophen
0113-1889	good sense pain relief	acetaminophen
0113-1975	Good Sense Pain Relief	Acetaminophen
0031-9301	Robitussin Direct Sore Throat Pain	acetaminophen