S-Oint DIAPER RASH AND SKIN PROTECTANT

Product NDC
73921-022
11-digit product format
739210022
Labeler code
73921
Product ID
73921-022_5cab9da5-5b41-4ff6-ac14-a5b6116a62dd
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
OINTMENT
Route
TOPICAL
Labeler
GLOBAL PHARMA HEALTHCARE PRIVATE LIMITED
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-04-01
Marketing end
0000-00-00
Substance
ZINC OXIDE
Active strength
400 mg/g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73921-022-302023-02-08C16284748780-1f386c64a-247f-0266-e053-dadaa90a7c1a155adc05-0420-476f-91a7-95241eb519c7
73921-022-302023-01-30C16284748780-1f386c64a-247f-0266-e053-dadaa90a7c1a155adc05-0420-476f-91a7-95241eb519c7

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73921-022-30739210022301 TUBE in 1 CARTON (73921-022-30) > 30 g in 1 TUBE1 tube2021-04-010000-00-00NoNoCurrent