NDC 15631-0384

SALICYLICUM ACIDUM

Salicylicum Acidum

SALICYLICUM ACIDUM is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Salicylic Acid.

Product ID15631-0384_a1bf6159-7fe8-ccd4-e053-2995a90a4d82
NDC15631-0384
Product TypeHuman Otc Drug
Proprietary NameSALICYLICUM ACIDUM
Generic NameSalicylicum Acidum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameSALICYLIC ACID
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0384-0

100 PELLET in 1 PACKAGE (15631-0384-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0384-4 [15631038404]

SALICYLICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0384-2 [15631038402]

SALICYLICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0384-1 [15631038401]

SALICYLICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0384-0 [15631038400]

SALICYLICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0384-3 [15631038403]

SALICYLICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0384-5 [15631038405]

SALICYLICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

Drug Details

Active Ingredients

IngredientStrength
SALICYLIC ACID3 [hp_X]/1

OpenFDA Data

SPL SET ID:8e73e9ec-a19b-449f-82f3-fec0511f5c53
Manufacturer
UNII

NDC Crossover Matching brand name "SALICYLICUM ACIDUM" or generic name "Salicylicum Acidum"

NDCBrand NameGeneric Name
0220-4526Salicylicum acidumSALICYLIC ACID
0220-4528Salicylicum acidumSALICYLIC ACID
15631-0384SALICYLICUM ACIDUMSALICYLICUM ACIDUM
68428-615Salicylicum acidumSALICYLIC ACID
71919-602SALICYLICUM ACIDUMSalicylic acid

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