Label: ALLERGY RELIEF NOW CHEMICAL SENSITIVITY REMEDY- chemical sensitivity remedy spray
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Contains inactivated NDC Code(s)
NDC Code(s): 61727-050-30 - 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 March 24, 2014
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- Active Ingredients:
- Suggested Use:
- PURPOSE
- Inactive Ingredients:
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- Allergy Relief Now Chemical Sensitivity Remedy 1 fl oz
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF NOW CHEMICAL SENSITIVITY REMEDY
chemical sensitivity remedy sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61727-050 Route of Administration oral Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC CATION (3+) 10 [hp_X] in 1 [hp_X] PHENOL (UNII: 339NCG44TV) (PHENOL - UNII:339NCG44TV) PHENOL 10 [hp_X] in 1 [hp_X] EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (EUPHORBIA RESINIFERA RESIN - UNII:1TI1O9028K) EUPHORBIA RESINIFERA RESIN 6 [hp_X] in 1 [hp_X] CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 10 [hp_X] in 1 [hp_X] HISTAMINE (UNII: 820484N8I3) (HISTAMINE - UNII:820484N8I3) HISTAMINE 12 [hp_X] in 1 [hp_X] GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 6 [hp_X] in 1 [hp_X] STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (STRYCHNOS IGNATII SEED - UNII:1NM3M2487K) STRYCHNOS IGNATII SEED 6 [hp_X] in 1 [hp_X] SODIUM CARBONATE (UNII: 45P3261C7T) (CARBONATE ION - UNII:7UJQ5OPE7D) SODIUM CARBONATE 10 [hp_X] in 1 [hp_X] NUTMEG (UNII: AEE24M3MQ9) (NUTMEG - UNII:AEE24M3MQ9) NUTMEG 6 [hp_X] in 1 [hp_X] STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 6 [hp_X] in 1 [hp_X] SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF) SULFURIC ACID 10 [hp_X] in 1 [hp_X] Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61727-050-30 1 [hp_X] in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/24/2014 Labeler - Homeocare Laboratories (088248828) Registrant - Homeocare Laboratories (088248828) Establishment Name Address ID/FEI Business Operations Homeocare Laboratories 088248828 manufacture(61727-050)