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Data / Drug companies / American Sales Company

American Sales Company: 136 products in the FDA NDC directory, labeler code 41520

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

American Sales Company (labeler code 41520) lists 136 products in the FDA National Drug Code Directory, covering 66 finished drugs by generic name. By type: 136 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on December 31, 2024.

The request: Watch American Sales Company (FDA labeler code 41520): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
41520
Products in commercial distribution
136
Packages
186
Finished drugs by generic name
66
Prescription products
0
Over the counter products
136
Flagged as original packager
123 of 123 products that carry the flag
Started marketing in the last 12 months
0
Products with a marketing end date set
1
Earliest marketing start
August 31, 1993
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs7051.5%
Generic drugs (ANDA)6144.9%
New drug applications (NDA)32.2%
Other unapproved drugs21.5%

Products by type

TypeProductsShare
Over the counter drugs136100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Acetaminophen12214
Ibuprofen10190
Nicotine polacrilex1057
Menthol5263
Loratadine4125
Naproxen sodium4100
Diphenhydramine hydrochloride4127
Omeprazole3106
Cetirizine hcl348
Miconazole nitrate3101
Hydrocortisone2171
Fluoride213
Pseudoephedrine hcl229
Guaifenesin2123
Simethicone286
Acetaminophen, dextromethorphan hbr, doxylamine succinate240
Oxymetazoline hydrochloride264
Fluticasone propionate271
Psyllium husk214
Acetaminophen, diphenhydramine hcl242
Dextromethorphan polistirex227
Calcium carbonate2101
Sodium bicarbonate, sodium chloride212
Cetirizine hydrochloride2119
Famotidine2138
Benzocaine1110
Liquid corn and callus remover18
Phenylephrine hydrochloride177
Diphenhydramine citrate and ibuprofen17
Bacitracin zinc, neomycin sulfate, polymyxin b sulfate144
Diphenhydramine hcl199
Dextromethorphan hbr, guaifenesin167
Cetylpyridinium chloride147
Clotrimazole198
Acetaminophen, aspirin, caffeine148
Jock itch spray talc free11
Salicylic acid 2%118
Aspirin1134
Fexofenadine hcl139
Polyethylene glycol 3350167
Tioconazole116
Diclofenac sodium1109
Loperamide hydrochloride182
Esomeprazole126
Isopropyl alcohol1177
Acetaminophen, dextromethorphan hbr, phenylephrine hcl145
Foot odor control spray13
Loperamide hydrochloride, simethicone120
Burn relief13
Aspirin, citric acid, sodium bicarbonate119
Stannous fluoride134
Liquid bandage116
Famotidine, calcium carbonate and magnesium hydroxide120
Famotidine, calcium carbonate, magnesium hydroxide114
Doxylamine succinate139
Loperamide hcl142
Dextromethorphan hbr, doxylamine succinate112
Mineral oil, petrolatum, phenylephrine hcl128
Medicated callus removers110
Witch hazel163
Diphenhydramine hydrochloride, naproxen sodium112
Medicated corn removers113
Anti-fungal miconazole athletes foot spray talc free11
Wart remover gel14
Liquid wart remover110
Sodium monofluorophosphate153

Dosage forms

Dosage formProductsShare
Tablet, film coated1914%
Suspension128.8%
Solution118.1%
Lozenge107.4%
Capsule, liquid filled96.6%
Tablet85.9%
Tablet, chewable75.1%
Gum, chewing64.4%
Tablet, coated53.7%
Cream42.9%
Paste, dentifrice42.9%
Liquid42.9%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
All Day Allergy41520-212Capsule, liquid filledGeneric drugs (ANDA)December 31, 2024
Soft Tip Neti Pot Sinus wash CareOne41520-929KitOther unapproved drugsJanuary 9, 2022
All natural Saline Packets CareOne41520-938Powder, for solutionOther unapproved drugsJanuary 8, 2022
Careone allergy relief41520-510Tablet, orally disintegratingGeneric drugs (ANDA)November 8, 2021
CareOne Allergy Relief41520-715Capsule, liquid filledGeneric drugs (ANDA)August 3, 2021
Careone omeprazole41520-802Tablet, delayed releaseNew drug applications (NDA)March 11, 2021
CareOne arthritis pain relief41520-788GelGeneric drugs (ANDA)October 29, 2020
Careone naproxen sodium pm41520-264Tablet, film coatedGeneric drugs (ANDA)February 25, 2020
Careone miconazole 141520-616KitGeneric drugs (ANDA)January 15, 2020
Careone triple antibiotic41520-067OintmentOver the counter monograph drugsOctober 1, 2019
Careone triple antibiotic41520-679OintmentOver the counter monograph drugsSeptember 26, 2019
Careone childrens allergy relief41520-553Spray, meteredGeneric drugs (ANDA)August 23, 2019
Allergy Relief41520-290Tablet, coatedOver the counter monograph drugsAugust 1, 2019
Careone childrens ibuprofen41520-740Tablet, chewableGeneric drugs (ANDA)July 24, 2019
Careone childrens allergy relief41520-716Tablet, chewableGeneric drugs (ANDA)July 16, 2019
Careone childrens ibuprofen41520-633Tablet, chewableGeneric drugs (ANDA)July 8, 2019
Careone miconazole 741520-825CreamGeneric drugs (ANDA)May 29, 2019
CAREONE Extra Strength Assorted Fruits41520-905Tablet, chewableOver the counter monograph drugsApril 19, 2019
CAREONE Orange Flavored41520-515PowderOver the counter monograph drugsApril 18, 2019
Careone41520-907CapsuleOver the counter monograph drugsApril 16, 2019
Natures Promise Childrens Fluoride Strawberry41520-724Paste, dentifriceOver the counter monograph drugsFebruary 11, 2019
Care One Restore and Defend Sensitive Whitening41520-722Paste, dentifriceOver the counter monograph drugsFebruary 11, 2019
CareOne Diarrhea and Gas Control41520-772TabletGeneric drugs (ANDA)January 31, 2019
Mucus Relief Maximum Strength41520-732TabletGeneric drugs (ANDA)December 31, 2018
Mucus Relief Extended Release41520-731TabletGeneric drugs (ANDA)December 31, 2018

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.