Product NDC: | 68703-005 |
Proprietary Name: | Skin Dr |
Non Proprietary Name: | Galium, Kali mur, Kali sulph, Nat mur, Urtica ur, Acacia gum, lactose, magnesium stearate, corn starch, sucrose |
Active Ingredient(s): | 3; 6; 6; 6; 6 [hp_X]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 & nbsp; Galium, Kali mur, Kali sulph, Nat mur, Urtica ur, Acacia gum, lactose, magnesium stearate, corn starch, sucrose |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68703-005 |
Labeler Name: | Native Remedies LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20130115 |
Package NDC: | 68703-005-80 |
Package Description: | 180 TABLET in 1 BOTTLE, GLASS (68703-005-80) |
NDC Code | 68703-005-80 |
Proprietary Name | Skin Dr |
Package Description | 180 TABLET in 1 BOTTLE, GLASS (68703-005-80) |
Product NDC | 68703-005 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Galium, Kali mur, Kali sulph, Nat mur, Urtica ur, Acacia gum, lactose, magnesium stearate, corn starch, sucrose |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20130115 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Native Remedies LLC |
Substance Name | GALIUM APARINE; POTASSIUM CHLORIDE; POTASSIUM SULFATE; SODIUM CHLORIDE; URTICA URENS |
Strength Number | 3; 6; 6; 6; 6 |
Strength Unit | [hp_X]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 |
Pharmaceutical Classes |