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NDC 49726-0040-60 Respitrol 10; 10; 10; 10; 10; 10; 10; 10; 10 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 Details
Respitrol 10; 10; 10; 10; 10; 10; 10; 10; 10 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Respitrol is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by HelloLife, Inc.. The primary component is ACTIVATED CHARCOAL; AMMONIUM CARBONATE; ANTIMONY POTASSIUM TARTRATE; BROMINE; CHLORINE; LOBELIA INFLATA; POTASSIUM CARBONATE; SULFURIC ACID; TIN.
Product Information
NDC | 49726-0040 |
---|---|
Product ID | 49726-040_082b8f9f-aca5-50b3-e063-6394a90adb1f |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Respitrol |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Ammonium Carbonicum, Antimonium Tartaricum, Bromium, Carbo Vegetabilis, Chlorinum, Kali Carbonicum, Lobelia Inflata, Stannum Metallicum, Sulphuricum Acidum |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET |
Route | ORAL |
Active Ingredient Strength | 10; 10; 10; 10; 10; 10; 10; 10; 10 |
Active Ingredient Units | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
Substance Name | ACTIVATED CHARCOAL; AMMONIUM CARBONATE; ANTIMONY POTASSIUM TARTRATE; BROMINE; CHLORINE; LOBELIA INFLATA; POTASSIUM CARBONATE; SULFURIC ACID; TIN |
Labeler Name | HelloLife, Inc. |
Pharmaceutical Class | n/a |
DEA Schedule | n/a |
Marketing Category | UNAPPROVED HOMEOPATHIC |
Application Number | n/a |
Listing Certified Through | 2024-12-31 |
Package
NDC 49726-0040-60 (49726004060)
NDC Package Code | 49726-040-60 |
---|---|
Billing NDC | 49726004060 |
Package | 60 TABLET in 1 BOTTLE, PLASTIC (49726-040-60) |
Marketing Start Date | 2018-06-15 |
NDC Exclude Flag | N |
Pricing Information | N/A |