Label: HANGOVER RELIEF- asafetida,capsicum,potassium dichromate,cola nut,lachesis muta venom,strychnos nux-vomica seed,ranunculus bulbosus,sulfuric acid,zinc. pellet
- NDC Code(s): 61727-330-21
- Packager: Homeocare Laboratories
- Category: HUMAN OTC DRUG LABEL
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 December 18, 2018
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- Official Label (Printer Friendly)
- Active ingredients:(HPUS)
- Purpose:
- Keep out of reach of children.
- Uses:
- Warnings:
- Inactive ingredients:
- Dosage & Administration:
- Hangover Relief
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INGREDIENTS AND APPEARANCE
HANGOVER RELIEF
asafetida,capsicum,potassium dichromate,cola nut,lachesis muta venom,strychnos nux-vomica seed,ranunculus bulbosus,sulfuric acid,zinc. pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61727-330 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASAFETIDA (UNII: W9FZA51AS1) (ASAFETIDA - UNII:W9FZA51AS1) ASAFETIDA 5 [hp_C] in 4 g CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG) CAPSICUM 5 [hp_C] in 4 g POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 5 [hp_C] in 4 g COLA NUT (UNII: PQM9SA369U) (COLA NUT - UNII:PQM9SA369U) COLA NUT 5 [hp_C] in 4 g LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 5 [hp_C] in 4 g STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 5 [hp_C] in 4 g RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB) (RANUNCULUS BULBOSUS - UNII:AEQ8NXJ0MB) RANUNCULUS BULBOSUS 7 [hp_C] in 4 g SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF) SULFURIC ACID 5 [hp_C] in 4 g ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC 5 [hp_C] in 4 g Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) LACTOSE (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61727-330-21 4 g in 1 TUBE; Type 0: Not a Combination Product 11/23/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/23/2011 Labeler - Homeocare Laboratories (088248828) Registrant - Homeocare Laboratories (088248828) Establishment Name Address ID/FEI Business Operations Homeocare Laboratories 088248828 manufacture(61727-330)