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Pain Relief Extra Strength
Pain Relief Extra Strength - 37808-195-12 - (Acetaminophen)
Drug Information of Pain Relief Extra Strength
| Product NDC: | 37808-195 |
| Proprietary Name: | Pain Relief Extra Strength |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 500 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, GELATIN COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pain Relief Extra Strength
| Product NDC: | 37808-195 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20040510 |
Package Information of Pain Relief Extra Strength
| Package NDC: | 37808-195-12 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (37808-195-12) > 100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC |
NDC Information of Pain Relief Extra Strength
| NDC Code | 37808-195-12 |
| Proprietary Name | Pain Relief Extra Strength |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (37808-195-12) > 100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC |
| Product NDC | 37808-195 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | CAPSULE, GELATIN COATED |
| Route Name | ORAL |
| Start Marketing Date | 20040510 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H E B |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
