NDC 61727-331

Acid Reflux Relief

Capsicum, Sodium Phosphate, Dibasic, Heptahydrate, Strychnos Nux-vomica Seed, Robinia Pseudoacacia Bark, Sulfur, Sepia Officinalis Juice

Acid Reflux Relief is a Sublingual Pellet in the Human Otc Drug category. It is labeled and distributed by Homeocare Laboratories. The primary component is Capsicum; Sodium Phosphate, Dibasic, Heptahydrate; Strychnos Nux-vomica Seed; Robinia Pseudoacacia Bark; Sulfur; Sepia Officinalis Juice.

Product ID61727-331_848ca4be-1f89-b274-e053-2a91aa0ad774
NDC61727-331
Product TypeHuman Otc Drug
Proprietary NameAcid Reflux Relief
Generic NameCapsicum, Sodium Phosphate, Dibasic, Heptahydrate, Strychnos Nux-vomica Seed, Robinia Pseudoacacia Bark, Sulfur, Sepia Officinalis Juice
Dosage FormPellet
Route of AdministrationSUBLINGUAL
Marketing Start Date2012-06-08
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHomeocare Laboratories
Substance NameCAPSICUM; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; STRYCHNOS NUX-VOMICA SEED; ROBINIA PSEUDOACACIA BARK; SULFUR; SEPIA OFFICINALIS JUICE
Active Ingredient Strength7 [hp_C]/4g; [hp_X]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 61727-331-21

4 g in 1 TUBE (61727-331-21)
Marketing Start Date2012-06-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 61727-331-21 [61727033121]

Acid Reflux Relief PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-06-08

Drug Details

Active Ingredients

IngredientStrength
CAPSICUM7 [hp_C]/4g

OpenFDA Data

SPL SET ID:01ddf3ee-e925-404d-9b41-7876d5fd6634
Manufacturer
UNII
UPC Code
  • 0361727331212
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