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Listings are compiled from public records — the NPPES national provider registry and the FDA National Drug Code Directory. Pharmacy Flow does not verify unclaimed listings and publishes no pricing for them.

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Directory/H E B

H E B

Drug manufacturer · manufacturer

Unclaimed listing
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257
Drug products
10
Therapeutic areas

About

H E B is listed in the FDA National Drug Code Directory with 257 marketed products. Dosage forms include SPRAY, CREAM, LIQUID, SOLUTION/ DROPS, JELLY.

What H E B makes

15 of 257 products
Clear
OTC · 257
Other · 130Dermatology · 47Immunology & Inflammation · 32Gastrointestinal · 12Nutrition & Supplements · 11Anti-infective · 10Respiratory & Allergy · 6CNS & Psychiatry · 4Pain & Anesthesia · 4Ophthalmic · 1
tablet · 74liquid · 29solution · 25capsule · 19suspension · 18cream · 15gum · 12lozenge · 10mouthwash · 10shampoo · 7
  • Athletes Foot Ultra
    butenafine hydrochloride
    QuotecreamtopicalANDA
  • HEB
    clotrimazole
    QuotecreamtopicalOTC MONOGRAPH DRUG
  • Colloidal oatmeal
    colloidal oatmeal
    QuotecreamtopicalOTC MONOGRAPH DRUG
  • itch relief
    diphenhydramine hydrochloride, zinc acetate
    QuotecreamtopicalOTC MONOGRAPH DRUG
  • Cold Sore Fever Blister
    docosanol
    QuotecreamtopicalANDA
  • Cold Sore Treatment
    docosanol
    QuotecreamtopicalANDA
  • Cold Sore Fever Blister Treatment
    docosanol
    QuotecreamtopicalANDA
  • Cold Sore Fever Blister
    docosanol
    QuotecreamtopicalANDA
  • hydrocortisone
    hydrocortisone
    QuotecreamtopicalOTC MONOGRAPH DRUG
  • Hydrocortisone
    hydrocortisone
    QuotecreamtopicalOTC MONOGRAPH DRUG
  • hydrocortisone
    hydrocortisone
    QuotecreamtopicalOTC MONOGRAPH DRUG
  • Miconazole
    miconazole nitrate
    QuotecreamvaginalANDA
  • miconazole 7
    miconazole nitrate
    QuotecreamvaginalANDA
  • antibiotic
    neomycin, polymyxin b, pramoxine hcl
    QuotecreamtopicalOTC MONOGRAPH DRUG
  • Athletes Foot
    terbinafine hydrochloride
    QuotecreamtopicalANDA

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Contact

Email and website are not published in the public registries — they are added when the listing is claimed.

From the FDA NDC Directory, refreshed 2026-08-15.

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