NDC 58264-0208

N-10

Sodium Chloride, Oyster Shell Calcium Carbonate, Crude, Sepia Officinalis Juice, Iodine, Lycopodium Clavatum Whole, And Bos Taurus Pituitary Gland, Posterior

N-10 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Sodium Chloride; Oyster Shell Calcium Carbonate, Crude; Sepia Officinalis Juice; Iodine; Lycopodium Clavatum Whole; Bos Taurus Pituitary Gland, Posterior.

Product ID58264-0208_9f3e0faa-f6cb-41a2-a172-e8ae4b379f6a
NDC58264-0208
Product TypeHuman Otc Drug
Proprietary NameN-10
Generic NameSodium Chloride, Oyster Shell Calcium Carbonate, Crude, Sepia Officinalis Juice, Iodine, Lycopodium Clavatum Whole, And Bos Taurus Pituitary Gland, Posterior
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameSODIUM CHLORIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SEPIA OFFICINALIS JUICE; IODINE; LYCOPODIUM CLAVATUM WHOLE; BOS TAURUS PITUITARY GLAND, POSTERIOR
Active Ingredient Strength30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 58264-0208-1

29.57 mL in 1 BOTTLE, GLASS (58264-0208-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0208-1 [58264020801]

N-10 SOLUTION
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SODIUM CHLORIDE30 [hp_X]/mL

OpenFDA Data

SPL SET ID:264d8093-70f3-43a5-bfc4-b719bb3e45e6
Manufacturer
UNII
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