Label: RELIEF 3-G12- acetylcholine chloride, histamine, interferon gamma-1a, interleukin-12 human, serotonin spray
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Contains inactivated NDC Code(s)
NDC Code(s): 63776-454-14 - Packager: VIATREXX BIO INCORPORATED
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated November 30, 2022
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- Active Ingredients
- Purpose:
- Uses
- Warnings
- Dosage
- Inactive Ingredients
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Principal Display Panel
VPC0611
NDC 63776-454-14
Homeopathic remedy
Relief 3-G12
• For symptoms due to sensitivity or reactions.
Oral spray
30ml 1 oz
Viatrexx™ Bio Incorporated
Manufactured by Viatrexx
www.viatrexx.com
Newark, DE 19713
Relief 3-G12
30 mL
1 oz
Viatrexx™ Bio Incorporated
ITEM: VPC0611
NDC: 63776-454-14
INDICATIONS:
For symptoms due to sensitivity or reactions.
DIRECTIONS:
1-3 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner.
Mfg. for
Viatrexx Bio Incorporated.
www.viatrexx.com
Newark, DE 19713
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INGREDIENTS AND APPEARANCE
RELIEF 3-G12
acetylcholine chloride, histamine, interferon gamma-1a, interleukin-12 human, serotonin sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63776-454 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETYLCHOLINE CHLORIDE (UNII: AF73293C2R) (ACETYLCHOLINE - UNII:N9YNS0M02X) ACETYLCHOLINE CHLORIDE 200 [kp_C] in 1 mL HISTAMINE (UNII: 820484N8I3) (HISTAMINE - UNII:820484N8I3) HISTAMINE 200 [kp_C] in 1 mL INTERFERON GAMMA-1A (UNII: VC9M78242P) (INTERFERON GAMMA-1A - UNII:VC9M78242P) INTERFERON GAMMA-1A 200 [kp_C] in 1 mL INTERLEUKIN-12 HUMAN (UNII: 7B590791ER) (INTERLEUKIN-12 HUMAN - UNII:7B590791ER) INTERLEUKIN-12 HUMAN 200 [kp_C] in 1 mL SEROTONIN (UNII: 333DO1RDJY) (SEROTONIN - UNII:333DO1RDJY) SEROTONIN 200 [kp_C] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63776-454-14 1 in 1 BOX 07/24/2012 1 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/24/2012 Labeler - VIATREXX BIO INCORPORATED (078419880) Establishment Name Address ID/FEI Business Operations Les Importations Herbasante Inc 243254612 manufacture(63776-454)